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Meijer Cold Therapy Citrus Flavor ZINC GLUCONATE 1 [hp_X]/1 Tablet, 25-count — NDC 41250-0936-25 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Meijer Cold Therapy Citrus Flavor ZINC GLUCONATE 1 [hp_X]/1 Tablet, 25-count — NDC 41250-936-25 (Billing 41250-0936-25)

by Meijer Distribution Inc · 25 TABLET in 1 BOTTLE, PLASTIC

This is a package of 25 tablets of Meijer Cold Therapy Citrus Flavor ZINC GLUCONATE 1 [hp_X]/1 Tablet from Meijer Distribution Inc, marketed since Apr 2019 and currently FDA-listed. It is this product's only package size.

NDC 41250-0936-25
🏷️ FDA NDC (as labeled) 41250-936-25 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41250-936-25
Product NDC 41250-936
11-digit billing NDC 41250093625
UNII U6WSN5SQ1Z
SPL Set ID d2629578-c0a4-417c-9b60-f4bad617321f
Established class (EPC) Copper Absorption Inhibitor
Physiologic effect Decreased Copper Ion Absorption
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-04-18
Route ORAL
Dosage form TABLET
Substance ZINC GLUCONATE
Why two NDCs? The FDA registers this code as 41250-936-25 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 41250-0936-25. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

This is an unapproved homeopathic oral tablet flavored with citrus that contains zinc gluconate. In homeopathic practice, zinc gluconate is traditionally used to support immune function and may be included in products marketed for cold symptoms. Homeopathic products are based on traditional use rather than clinical evidence and have not been evaluated by the FDA for safety or effectiveness.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
41250-0936-25 You're viewing this Main listing 25 TABLET in 1 BOTTLE, PLASTIC 2019-04-18 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Zinc Cold Therapy 1 [hp_X] 63868-0287-25 Chain 25 tablets — — FDA listed —
CVS Health Cold Remedy Citrus Flavor 1 [hp_X] 69842-0688-25 CVS 25 tablets — — FDA listed —
Zinc 1 [hp_X] 49035-0881-25 Wal-Mart 25 tablets — — FDA listed —
Premier Value Zinc Cold Therapy Citrus Flavor 1 [hp_X] 68016-0118-25 PHARMACY 25 tablets — — FDA listed —
Zinc Cold Therapy 1 [hp_X] 70000-0391-01 CARDINAL 25 tablets — — Discontinued —
Zinc Cold therapy 1 [hp_X] 30142-0999-25 THE 25 tablets — — FDA listed —
TopCare Zinc Cold Remedy Citrus Flavor 1 [hp_X] 36800-0806-25 TOPCO 25 tablets — — FDA listed —
Meijer Cold Therapy Citrus Flavor 1 [hp_X]this 41250-0936-25 Meijer 25 tablets — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2019
On the market since
Apr 2019
📍
2026
Currently FDA-listed
7 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color Orange
ShapeRound
ImprintRP118
Size16 mm
ScoringNot scored
FlavorCitrus
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII PQ6CK8PD0R
    Ascorbic acid, also known as vitamin C, is a white crystalline powder. It serves as an antioxidant to prevent degradation of other ingredients and may also function as a preservative in the formulation.
  • UNII 2S7830E561
    Crospovidone is a synthetic polymer derived from povidone. It acts as a disintegrant, helping the tablet or capsule break apart quickly in the stomach so the active ingredient can be absorbed.
  • UNII H77VEI93A8
    A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
  • UNII 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
  • UNII 96K6UQ3ZD4
    Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.

7 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesascorbic acid, crospovidone, FD&C Yellow No. 6, flavors, magnesium stearate, sorbitol, starch, sucralose.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerMeijer Distribution Inc
Labeler code41250
First marketedApr 2019
Product typeHuman Otc Drug
Portfolio245 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 121 words ▾

Uses may help reduce duration of cold symptoms: sore throat stuffy nose sneezing coughing This product was formulated to help reduce the duration and severity of cold symptoms and was not formulated to be effective for flu or allergies. Warnings Ask a doctor before use if you have a sensitivity to zinc or are allergic zinc are taking minocycline, doxycycline, tetracycline or are on Coumadin therapy, zinc treatment may inhibit the absorption of these medicines. Stop Use and ask a doctor If symptoms persist beyond 7 days.

If pregnant or breast feeding As ask health professional before use. Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

⏱️ Dosage and Administration 119 words ▾

Directions for best results, use at the first sign of a cold and continue to use as directed adults and children 12 years of age and older: chew one tablet completely at the onset of symptoms. Do not swallow tablets whole. repeat every 3 hours until symptoms are gone to avoid minor stomach upset, do not take on an empty stomach. do not eat or drink for 15 minutes after use. Do not eat or drink citrus fruits or juices for 30 minutes before or after use.

Otherwise, drink plenty of fluids. recommended daily dose is 6 tablets for adults and 4 tablets for ages 12 through 17 Children under 12 years of age: Consult a doctor before use.

⚠️ Warnings 82 words ▾

Warnings Ask a doctor before use if you have a sensitivity to zinc or are allergic zinc are taking minocycline, doxycycline, tetracycline or are on Coumadin therapy, zinc treatment may inhibit the absorption of these medicines. Stop Use and ask a doctor If symptoms persist beyond 7 days. If pregnant or breast feeding As ask health professional before use.

Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

📦 Storage and Handling 21 words ▾

Other information Do not take zinc tablets on an empty stomach to avoid possible minor stomach upset. Store at room temperature

🧪 Active Ingredient 10 words ▾

Active Ingredient Zincum Gluconicum 1x (11mg Zinc) Purpose Cold Remedy

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients ascorbic acid, crospovidone, FD&C Yellow No. 6, flavors, magnesium stearate, sorbitol, starch, sucralose.

🎯 Purpose 3 words ▾

Purpose Cold Remedy

📄 Ask a Doctor Before Use If 81 words ▾

Ask a doctor before use if you have a sensitivity to zinc or are allergic zinc are taking minocycline, doxycycline, tetracycline or are on Coumadin therapy, zinc treatment may inhibit the absorption of these medicines. Stop Use and ask a doctor If symptoms persist beyond 7 days. If pregnant or breast feeding As ask health professional before use.

Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

📄 Stop Use and Ask a Doctor If 46 words ▾

Stop Use and ask a doctor If symptoms persist beyond 7 days. If pregnant or breast feeding As ask health professional before use. Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

🤰 If Pregnant or Breast-Feeding 34 words ▾

If pregnant or breast feeding As ask health professional before use. Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

📄 Keep Out of Reach of Children 23 words ▾

Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

📄 Questions or Comments 4 words ▾

Questions or comments? 1-866-467-2748

📄 Package Label / Principal Display Panel 176 words ▾

PRINCIPAL DISPLAY PANEL meijer ® NDC 41250-936-25 *Compare to Zicam ® Cold Remedy Rapid Melts ® Ionizable Zinc Content* Zinc cold therapy Zincum Gluconicum Citrus Flavor Naturally and Artificially Flavored May help reduce the duration of cold symptoms** Sugar Free Homeopathic† 25 Chewable Tablets DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING. †CLAIM IS BASED ONLY ON THEORIES OF HOMEOPATHY FROM 1700S NOT ACCEPTED BY MOST MODERN MEDICAL EXPERTS .THERE IS NO SCIENTIFIC EVIDENCE THAT THE PRODUCT WORKS **THIS PRODUCT IS A HOMEOPATHIC REMEDY, AS SUCH, IT HAS NOT UNDERGONE REVIEW ON APPROVAL BY THE FDA AND THEREFORE HAS NOT BEEN DEMONSTRATED TO BE SAFE OR EFFECTIVE TO DIAGNOSE, TREAT, PREVENT, MITIGATE OR CURE ANY CONDITION OR DISEASE.

IMPORTANT: Keep this carton for future reference on full labeling. * This product is not manufactured or distributed by Zicam, LLC, owner of the registered trademarks Zicam ® Cold Remedy Rapidmelts ® OUR GUALITY GURANTEE DIST. BY: MEIJER DISTRIBUTION, INC GRAND RAPIDS, MI 49544 www.meijer.com meijer zinc cold therapy Zincum Gluconicum citrus flavor

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for ZINC GLUCONATE — the ingredient across all brands.

Top reported reactions

Fatigue2,769
Pain1,999
Nausea1,993
Diarrhoea1,987
Headache1,901
Dyspnoea1,550
Arthralgia1,388

Age at onset

Neonate50
Infant27
Child62
Adolescent69
Adult2,545
Elderly2,699

Reporter sex

26,582 reports
Male · 34%
Female · 66%
Unknown · 0%

Serious outcomes

Hospitalization6,610
Death1,591
Disabling1,374
Life-threatening1,124
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 3,140 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Meijer Cold Therapy Citrus Flavor ZINC GLUCONATE 1 [hp_X]/1 TABLET is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Meijer Distribution Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Meijer Distribution Inc is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 41250-0930-19 · Meijer 41250-0937-01 · Meijer →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.