Strong Evidence Mineral

Zinc

An essential trace mineral critical for immune function, wound healing, and protein synthesis.

Updated February 20, 2026

This content is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before starting, stopping, or changing any supplement or medication regimen.

Benefits & Uses

• Acute diarrhea (children): Strong evidence from multiple meta-analyses shows zinc supplementation reduces duration and stool volume in acute diarrheal illness, especially in populations with marginal zinc status. • Common cold: Meta-analyses suggest zinc acetate/gluconate lozenges started within 24 hours may shorten cold duration and reduce symptom severity; evidence is moderate and depends on formulation/dose. • Age-related macular degeneration (AMD): Large RCTs (AREDS/AREDS2) indicate zinc (with antioxidants and copper) slows progression of intermediate-to-advanced AMD; evidence is strong for progression risk reduction, not for primary prevention. • Wound healing: Evidence indicates zinc deficiency impairs healing; correcting deficiency and certain topical zinc preparations may aid healing; oral supplementation beyond repletion shows mixed-to-moderate evidence. • Taste/smell and immune support in deficiency: Zinc repletion improves dysgeusia and immune function when deficiency is present; evidence moderate. • Growth/development in malnourished children: Supplementation improves linear growth and reduces infections in zinc-deficient settings; evidence strong in low-resource populations.

Side Effects & Precautions

Common: nausea, abdominal cramps, vomiting, diarrhea, metallic taste, heartburn—more likely on an empty stomach or at doses ≥40 mg/day. Lozenges: mouth/throat irritation, bad taste, nausea. Less common: headache, dizziness, drowsiness. Dose-related effects with long-term high intake (generally ≥50 mg/day for weeks–months): copper deficiency (anemia, neutropenia), impaired immune function, decreased HDL cholesterol, possible neurologic symptoms (paresthesias/ataxia) secondary to copper deficiency. Rare but serious: permanent loss of smell (anosmia) from intranasal zinc products—avoid intranasal forms. Hypersensitivity reactions are rare.

Dosage & Administration

Typical supplemental doses: 5–25 mg elemental zinc/day for general supplementation; RDAs: adults—11 mg/day (men), 8 mg/day (women), with higher needs in pregnancy/lactation; Tolerable Upper Intake Level (UL): 40 mg/day for adults (lower for children). Cold treatment trials: lozenges providing ≥75–100 mg/day elemental zinc (often acetate or gluconate) divided over the day for ≤7–14 days; efficacy depends on adequate ionic zinc release and early initiation. Pediatric acute diarrhea: 10–20 mg/day for 10–14 days (per WHO/UNICEF guidance in low-resource settings). AMD (AREDS): 80 mg/day zinc oxide plus copper (to prevent deficiency) with antioxidants; used under ophthalmologist guidance. Formulations include zinc gluconate, acetate, sulfate, and picolinate; absorption can be reduced by phytates and concurrent iron/calcium/magnesium. Optimal dosing varies by individual status and indication; long-term high-dose use warrants copper monitoring.

Contraindications

• Known allergy to zinc or product excipients. • Existing copper deficiency or conditions at risk for copper deficiency—avoid high-dose zinc without medical supervision. • Concomitant use of interacting drugs where separation is not feasible (e.g., penicillamine for Wilson’s disease)—requires clinician guidance. • Pregnancy/lactation: Generally safe within RDA; avoid chronic high-dose supplementation unless prescribed. • Prostate health: Observational data link long-term high-dose supplemental zinc (>100 mg/day) with higher risk of advanced prostate cancer; avoid chronic high-dose use. • Kidney/liver impairment: Trace element homeostasis may be altered—use caution and medical oversight. • Surgery: No specific bleeding risk; disclose use. Avoid high-dose lozenges perioperatively due to nausea/aspiration risk. • Anticoagulation: Zinc does not appear to increase bleeding, but disclose to clinicians.

Known Interactions

Substance Type Severity Description
Tetracycline antibiotics (e.g., doxycycline) antagonistic moderate Zinc forms chelates with tetracyclines in the gut, reducing antibiotic and zinc absorption.
Fluoroquinolone antibiotics (e.g., ciprofloxacin, levofloxacin) antagonistic moderate Chelation in the GI tract decreases fluoroquinolone bioavailability and zinc absorption.
Penicillamine antagonistic severe Zinc markedly reduces penicillamine absorption and efficacy (used in RA/Wilson’s); dosing must be widely separated or avoided unless medically supervised.
Copper supplements/foods antagonistic moderate Zinc induces intestinal metallothionein, trapping copper and reducing its absorption; long-term high-dose zinc can cause copper deficiency.
Iron supplements (non-heme) antagonistic moderate Competition for shared transporters reduces absorption of both minerals, especially when taken together on an empty stomach.
Calcium/magnesium salts and antacids antagonistic mild Mineral salts and reduced gastric acidity can diminish zinc absorption via complex formation and pH effects.
Thiazide diuretics (e.g., hydrochlorothiazide) caution moderate May increase urinary zinc excretion, potentially lowering zinc status during long-term use.
Proton pump inhibitors (e.g., omeprazole) caution mild Reduced gastric acidity may lower zinc ionization and absorption; clinical impact likely small but possible in marginal status.

Check interactions with other supplements

Sources
  1. Zinc for the common cold (Cochrane Review) (meta-analysis) , 2013
  2. Zinc acetate lozenges for treating the common cold: meta-analysis of randomized trials (meta-analysis) , 2017
  3. Zinc supplementation for acute diarrhea in children (Cochrane Review) (meta-analysis) , 2016
  4. A randomized, placebo-controlled clinical trial of antioxidants and zinc for AMD (AREDS Report No. 8) (rct) , 2001
  5. Lutein/zeaxanthin and omega-3 in AMD: the AREDS2 randomized clinical trial (rct) , 2013
  6. Zinc and wound healing: physiology and clinical applications (review) (review) , 2014

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Health Disclaimer

This content is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before starting, stopping, or changing any supplement or medication regimen.