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Rite Aid Zinc Cold Therapy Zincum Gluconicum 1 [hp_X]/1 Tablet, 25-count — NDC 11822-1183-5 (Billing 11822-1183-05)

by RITE AID CORPORATION · 25 TABLET in 1 BOTTLE, PLASTIC

This is a package of 25 tablets of Rite Aid Zinc Cold Therapy Zincum Gluconicum 1 [hp_X]/1 Tablet from RITE AID CORPORATION, marketed since Apr 2020 and currently FDA-listed. It is this product's only package size.

NDC 11822-1183-05
🏷️ FDA NDC (as labeled) 11822-1183-5 billing pads the package 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) 11822-1183-5
Product NDC 11822-1183
11-digit billing NDC 11822118305
UNII U6WSN5SQ1Z
SPL Set ID c3744b40-9dae-4f40-955d-c7a7b596ee6e
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 2020-04-13
Route ORAL
Dosage form TABLET
Substance ZINC GLUCONATE
Why two NDCs? The FDA registers this code as 11822-1183-5 — a 5-4-1 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 package segment → 11822-1183-05. 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?

Rite Aid Zinc Cold Therapy is an oral tablet containing zinc gluconate marketed as a homeopathic product. In homeopathic practice, zinc is traditionally used to support immune function and reduce cold symptoms, though homeopathic products are not evaluated by the FDA for effectiveness. This product is formulated and marketed based on homeopathic tradition rather than clinical evidence of safety or efficacy.

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
11822-1183-05 You're viewing this Main listing 25 TABLET in 1 BOTTLE, PLASTIC 2020-04-13 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
TopCare Health Cold Remedy Cherry Flavor 1 [hp_X] 36800-0805-25 TOPCO 25 tablets — — FDA listed —
Rite Aid Zinc Cold Therapy 1 [hp_X]this 11822-1183-05 RITE 25 tablets — — FDA listed —
CVS Health Cold Remedy Cherry Flavor 1 [hp_X] 69842-0687-25 CVS 25 tablets — — FDA listed —
CVS Health Cold Remedy Orange Cream Flavor 1 [hp_X] 69842-0691-18 CVS 18 tablets — — FDA listed —
CVS Health Cold Remedy Lemon Flavor 1 [hp_X] 69842-0690-25 CVS 25 tablets — — FDA listed —
Zinc cold Remedy Non Drowsy 1 [hp_X] 79903-0054-25 WALMART 25 tablets — — FDA listed —
Walgreen Cold Therapy Cherry Flavor 1 [hp_X] 00363-1180-25 WALGREENS 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

🏛️
2020
On the market since
Apr 2020
📍
2026
Currently FDA-listed
6 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.

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerRITE AID CORPORATION
Labeler code11822
First marketedApr 2020
Product typeHuman Otc Drug
Portfolio326 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 128 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 127 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 84 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 23 words ▾

Other information ▪ do not take zinc tablets on an empty stomach to avoid possible minor stomach upset. ▪ store at room temperature

🧪 Active Ingredient 13 words ▾

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

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients ascorbic acid, crospovidone, flavors, magnesium stearate, sorbitol, starch ,sucralose.

🎯 Purpose 3 words ▾

Purpose Cold Remedy

📄 Ask a Doctor Before Use If 83 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 171 words ▾

PRINCIPAL DISPLAY PANEL NDC 11822-1183-5 *Compare to Ionizable Zinc Content in Zicam ® Cold Remedy Rapid Melts ® Zinc Cold Therapy ZINCUM GLUCONICUM May help reduce the duration of cold symptoms** Sugar Free Homeopathic† Cherry Flavor Naturally and Artificially Flavored 25 CHEWABLE TABLETS Package Contains One Bottle 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 Matrixx Initiatives, Inc., owner of the registered trademarks Zicam ® Cold Remedy Rapidmelts ® Distributed by: Rite Aid Zinc Cold Therapy Zincum Gluconicum 25 Chewable Tablets

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

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Rite Aid Zinc Cold Therapy Zincum Gluconicum 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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 RITE AID CORPORATION. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
RITE AID CORPORATION 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.
← 11822-1182-05 · RITE 11822-1189-00 · Rite →
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.