Skip to main content
Evidence Based Longevity (EBL) Check what I take
In plain words

Zinc is a mineral the body needs in small amounts. In adults, zinc lozenges shortened colds by about two and a half days. The effect came from lozenges giving about 80 to 90 milligrams a day, and a low-dose lozenge did not help. In children, zinc did not shorten colds. Taking high doses for a long time can drain the body's copper and cause anemia or nerve damage that does not always reverse.

The B belongs to one of the three uses graded on this record. The other two carry their own letters.

Grades by use · each use graded on its own evidence
BCommon-cold duration in adultsself-report
As studied, and the trials
As studied
DoseAbout 75 to 92 mg of zinc a day in the positive lozenge trials (Hemilä and Chalker 2015, PMID PubMed ID: the permanent number the US National Library of Medicine gives a published paper. Each one links to that paper's record on PubMed. 25888289); a 13 mg lozenge six times a day was null (Hemilä 2020, PMID 31980506).
FormZinc acetate or zinc gluconate lozenges dissolved in the mouth (Hemilä 2016, PMID 27378206; Hemilä and Chalker 2015, PMID 25888289); zinc in any oral form in the wider pool (Science 2012, PMID 22566526).
PopulationAdults with naturally acquired colds: 199 patients in 3 trials (Hemilä 2016, PMID 27378206); 2,121 participants of all ages in 17 trials, adults analyzed separately (Science 2012, PMID 22566526); 87 adults with colds (Hemilä 2020, PMID 31980506).
DurationLozenges started within 24 hours of the first symptoms and taken while symptoms lasted, usually up to about a week (Science 2012, PMID 22566526; Hemilä 2016, PMID 27378206).

Science et al. (CMAJ, 2012; PMID 22566526) found colds 2.63 days shorter in adults; Hemilä et al. (Br J Clin Pharmacol, 2016; PMID 27378206) found 2.73 days in individual patient data from 3 lozenge trials; Hemilä and Chalker (BMC Fam Pract, 2015; PMID 25888289) tie the effect to 80 to 92 mg a day; the 13 mg lozenge trial was null (Hemilä et al., BMJ Open, 2020; PMID 31980506). Replicated The same finding reproduced by a separate research group. A result seen once can be chance or bias; a replicated one is harder to explain away., on a self-reported endpoint The outcome a trial measures to decide whether the treatment worked, such as heart attacks, blood pressure or a symptom score., which caps the letter at B. The Cochrane review this record used to cite was withdrawn in 2015 and no longer supports anything here.

CCommon-cold duration in childrenself-report
As studied, and the trials
As studied
Dosenot stated in the cited abstract
FormOral zinc in the pediatric trials of the pool, forms varying by trial (Science 2012, PMID 22566526).
PopulationChildren with colds, analyzed as a subgroup of 17 trials (Science 2012, PMID 22566526).
Durationnot stated in the cited abstract

Science et al. (CMAJ, 2012; PMID 22566526): in children the pooled effect on cold duration was not significant (0.26 days shorter, 95% CI -0.25 to 0.78). Randomized evidence exists and it is not positive in this group, so the adult result does not transfer: C.

CSlowing progression to advanced age-related macular degeneration in people at high risk (zinc 80 mg with copper)blinded clinician rating
As studied, and the trials
As studied
Dose80 mg zinc with 2 mg copper a day (AREDS, PMID 11594942).
FormZinc oxide with cupric oxide, alone or with vitamin C, vitamin E and beta-carotene (AREDS, PMID 11594942).
Population3,640 adults aged 55 to 80 with signs of age-related macular degeneration (AREDS, PMID 11594942).
DurationAverage 6.3 years (AREDS, PMID 11594942).

AREDS (Age-Related Eye Disease Study Research Group, Arch Ophthalmol, 2001; PMID 11594942): 3,640 adults aged 55 to 80 with signs of macular degeneration, followed an average 6.3 years. Against placebo An inactive substitute made to look like the real treatment, so participants cannot tell which one they received., antioxidants plus zinc lowered the odds of advanced disease (odds ratio 0.72, 99% CI 0.52 to 0.98); zinc alone did not reach the trial's significance level overall (0.75, 0.55 to 1.03) and did once the 1,063 lowest-risk participants were set aside (0.71, 0.52 to 0.99). One trial, positive mainly for the combination and for zinc alone only in the higher-risk subgroup, and not repeated against placebo by an independent group: C. The photographs were graded by masked readers. This does not grade zinc for preventing macular degeneration in people without signs of it.

Read the grade that matches your goal. How EBL grades by use →

B Zinc structure
Elemental mineral · chelated form graded
Dose studied
75 mg/day (lozenge)
Form graded
Zinc picolinate or gluconate (forms used in trials)
B Grade B

A letter describes the human evidence, not the product, the manufacturer, or the ingredient's worth.

See the full evidence record →

Zinc lozenges for common-cold duration in adults, graded on published human trial evidence.

RCTWhy this flag? ▾

At least one randomized, placebo-controlled human trial, typically double-blinded Neither the participants nor the people assessing them know who received the real treatment until the trial ends..

Learn more about evidence flags →
PilotWhy this flag? ▾

Small (typically n<50), exploratory trial. Often open-label Everyone in the trial knows which treatment they are receiving, so expectations can shape the results, especially for symptoms people report themselves.. Hypothesis-generating, not definitive.

Learn more about evidence flags →
As studied: dose, form, population and duration for every use
As studied
Common-cold duration in adults
FormZinc acetate or zinc gluconate lozenges dissolved in the mouth (Hemilä 2016, PMID 27378206; Hemilä and Chalker 2015, PMID 25888289); zinc in any oral form in the wider pool (Science 2012, PMID 22566526).
DoseAbout 75 to 92 mg of zinc a day in the positive lozenge trials (Hemilä and Chalker 2015, PMID 25888289); a 13 mg lozenge six times a day was null (Hemilä 2020, PMID 31980506).
PopulationAdults with naturally acquired colds: 199 patients in 3 trials (Hemilä 2016, PMID 27378206); 2,121 participants of all ages in 17 trials, adults analyzed separately (Science 2012, PMID 22566526); 87 adults with colds (Hemilä 2020, PMID 31980506).
DurationLozenges started within 24 hours of the first symptoms and taken while symptoms lasted, usually up to about a week (Science 2012, PMID 22566526; Hemilä 2016, PMID 27378206).
Common-cold duration in children
FormOral zinc in the pediatric trials of the pool, forms varying by trial (Science 2012, PMID 22566526).
Dosenot stated in the cited abstract
PopulationChildren with colds, analyzed as a subgroup of 17 trials (Science 2012, PMID 22566526).
Durationnot stated in the cited abstract
Slowing progression to advanced age-related macular degeneration in people at high risk (zinc 80 mg with copper)
FormZinc oxide with cupric oxide, alone or with vitamin C, vitamin E and beta-carotene (AREDS, PMID 11594942).
Dose80 mg zinc with 2 mg copper a day (AREDS, PMID 11594942).
Population3,640 adults aged 55 to 80 with signs of age-related macular degeneration (AREDS, PMID 11594942).
DurationAverage 6.3 years (AREDS, PMID 11594942).

A grade describes the intervention that was tested. Where the product on the shelf differs from it, this says so.

How this letter has changed · latest: October 2026 · Added
Grade history
October 2026 · Added
Zinc: progression of age-related macular degeneration added at Grade C

AREDS (Age-Related Eye Disease Study Research Group, Arch Ophthalmol, 2001; PMID 11594942) found zinc 80 mg with copper, combined with antioxidants, slowed progression to advanced macular degeneration in 3,640 adults with signs of the disease; zinc alone reached significance only in the higher-risk group. One trial, not independently repeated against placebo, is C. The record's top letter does not change.PMID 11594942

October 2026 · Corrected
Zinc: the withdrawn Cochrane review replaced; B narrowed to adults taking high-dose lozenges

The zinc record rested on one citation, Singh and Das (Cochrane Database of Systematic Reviews A review that searches for every study on a question using a method set in advance, then assesses them together., 2013; PMID 23775705), which Cochrane withdrew in 2015. It is replaced by Science et al. (CMAJ, 2012; PMID 22566526), Hemilä et al. (Br J Clin Pharmacol, 2016; PMID 27378206), Hemilä and Chalker (BMC Fam Pract, 2015; PMID 25888289) and Hemilä et al. (BMJ Open, 2020; PMID 31980506). They agree that lozenges supplying about 75 to 92 mg of zinc a day, started early, shorten colds in adults by roughly two and a half days, that a 13 mg lozenge did not, and that children showed no significant effect. The B now names that use, form and dose; children are graded C; deficiency correction is no longer part of the graded use.PMID 23775705 PMID 22566526 PMID 27378206 PMID 25888289 PMID 31980506

Every change to a letter on this site is dated and published. The full evidence log →

Commercial disclosure
EBL earns no commission on any supplement it grades. A purchase made through the dispensary link below pays EBL nothing, the practitioner discount goes to you in full. The dispensary is Fullscript, a practitioner dispensary, and many of the professional-grade brands in it are sold mainly through practitioners rather than in health food stores. Grades are assigned by published rubric before any commercial relationship exists and are never influenced by one. Full disclosure.

Evidence last reviewed October 2026
Dose

No dose is published here. This record carries no authored dose, because the cited trials do not converge on a single figure. Each trial cited on this page states the dose it used, and EBL has not turned those into a recommendation.

Form note

Standardized forms were used in the cited trials; product quality varies.

Timing in the trials

The trial of the 13 mg lozenge had it taken six times a day (PMID 31980506). The pooled analyses give daily amounts from lozenges taken through the day and do not state clock times (PMID 22566526, PMID 27378206).

Checked against the published summaries; the full papers could not be read. What the cited trials did, not a schedule. Every supplement, by trial timing →

Contraindications A condition or medication that makes a treatment unsafe or unsuitable for a particular person. · read before use
Contraindications and cautions

Long-term use above the upper intake level without copper. Sustained high-dose zinc induces intestinal metallothionein, which traps copper and can produce a copper-deficiency anemia or a myelopathy that does not always reverse.

Drug Interactions

Quinolone and tetracycline antibiotics: zinc chelates them in the gut and reduces absorption of both, which is a separation-in-time problem. Penicillamine and bisphosphonates, the same way. Thiazide diuretics increase urinary zinc loss. Copper: the interaction that matters most here is with a nutrient rather than a drug.

Sources for the above

Sustained high-dose zinc causes copper deficiency. Prolonged high-dose zinc induces intestinal metallothionein and traps copper, producing copper-deficiency anemia and a myelopathy that does not reliably reverse on stopping. Kumar (Mayo Clinic Proceedings, 2006; PMID 17036563): copper deficiency myelopathy, case series and review. Jaiser and Winston (Journal of Neurology, 2010; PMID 20232210): review of copper deficiency myelopathy including the zinc-induced cases.

How to track

Serum zinc at baseline and 8 weeks: deficiency is common in older adults and the supplementation benefit is most pronounced when correcting a deficit. Also monitor copper levels at 12 weeks if supplementing above 15 mg/day, as zinc and copper compete for absorption. For immune applications, track frequency of upper respiratory infections over a 6-month period.

Primary evidenceFour papers, each linked to its PubMed record.
Primary evidence

Science et al. (CMAJ, 2012; PMID 22566526): meta-analysis A study that pools the numbers from several trials into one combined estimate. of 17 randomized trials, 2,121 participants; zinc shortened colds by 2.63 days in adults (95% CI 1.58 to 3.69 days) and had no significant effect in children (0.26 days, 95% CI -0.25 to 0.78), with very high heterogeneity How much the results of the pooled trials differ from each other. High heterogeneity makes a combined estimate less reliable.. Hemilä et al. (British Journal of Clinical Pharmacology, 2016; PMID 27378206): individual patient data from 3 randomized trials of zinc acetate lozenges, 199 patients; colds 2.73 days shorter. Hemilä and Chalker (BMC Family Practice, 2015; PMID 25888289): the effect comes from lozenges supplying 80 to 92 mg of zinc a day. Hemilä et al. (BMJ Open, 2020; PMID 31980506): a randomized trial of a 13 mg lozenge taken six times a day found no difference in recovery (rate ratio 0.68, 95% CI 0.42 to 1.08), so the dose matters. Grade B on self-reported cold duration in adults, which caps at B. Correcting zinc deficiency is not graded: no cited trial measured a clinical outcome in deficient people, and a rise in blood zinc is a level of the supplement itself.

Educational use only · Not medical advice · Starting, stopping or changing any supplement or medication is a decision for your physician

FDA / DSHEA statement

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. The grade on this page describes the strength of published human trial evidence in the populations studied. It is not a recommendation for any individual and is not medical advice. Starting, stopping or changing any supplement or medication is a decision for your physician.

Who responds?

Trials report an average. This box says whether any trial on this record looked at who the result applies to, and what it found.

For Slowing progression to advanced age-related macular degeneration in people at high risk (zinc 80 mg with copper), Grade C · Subgroup tested, effect differedAREDS (Age-Related Eye Disease Study Research Group, Arch Ophthalmol, 2001; PMID 11594942) found zinc alone short of significance across all 3,640 participants, and significant once the 1,063 at lowest risk of progression were set aside. The effect was seen in people already at higher risk of advanced disease. A subgroup result shows who the effect appeared in within these trials. It does not change the letter.

Independence
EBL earns nothing on this record.

This page carries a letter. EBL takes no commission, referral fee or payment of any kind on anything it grades. No letter has been bought and none is for sale.

How this is enforced

That is not a promise, it is a build condition. Two checks run on every deploy: one refuses to publish if a commission is claimed on anything graded, the other refuses if a page names a commercial relationship that is not declared in the register. If either fails, this page does not go live. You can read how the checks work, and what they do not cover, on the evidence integrity page.

How EBL searched for the trials (1 search)

The search that was run, what it returned, and what was left out and why, so the absence of evidence can be checked as well as its presence.

Searched PubMed in October 2026. 35 records screened, 19 eligible for the graded claim.
Query: zinc[tiab] AND "common cold"[tiab] AND (meta-analysis[pt] OR randomized controlled trial[pt])
Eligibility judged on titles: human RCTs Randomized controlled trial: people are assigned to the treatment or a comparison by chance, so the groups differ only in what they received. It is the design that can show cause and effect. or pooled analyses of oral zinc for treating the common cold. Abstracts read: Science 2012 (PMID 22566526), Hemila 2016 IPD (PMID 27378206), Hemila and Chalker 2015 (PMID 25888289), Hemila 2020 RCT (PMID 31980506), and the 2015 withdrawal notice for the cited Cochrane review (PMID 25924708). Screened out: intranasal zinc gel or spray trials (a different form), prevention-only trials, safety and glucose-control trials, methodological reanalyses, an off-topic pleuran trial, a crop-genetics paper, a pediatric anorexia trial and an overview of Cochrane reviews. Eligible count is title-based and approximate. Deficiency was not searched (one search per item).

Grades move when new trials publish. A free monthly email lists every grade EBL moved, with the reason and the trial behind it: the sign-up is on the Evidence Log →