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Meijer Extra Strength Freshmint Flavor Calcium Carbonate ,Magnesium Hydroxide 675 mg; 135 mg Tablet, Chewable, 100-count — NDC 41250-0978-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Meijer Extra Strength Freshmint Flavor Calcium Carbonate ,Magnesium Hydroxide 675 mg; 135 mg Tablet, Chewable, 100-count — NDC 41250-978-10 (Billing 41250-0978-10)

by MEIJER DISTRIBUTION INC · 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

This is a package of 100 tablets of Meijer Extra Strength Freshmint Flavor Calcium Carbonate ,Magnesium Hydroxide 675 mg; 135 mg Tablet, Chewable from MEIJER DISTRIBUTION INC, marketed since Apr 2019 and currently FDA-listed. It is this product's only package size.

NDC 41250-0978-10
🏷️ FDA NDC (as labeled) 41250-978-10 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 Oct 1, 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

NDC database record

One package, one record: these facts belong to NDC 41250-978-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
41250 labeler · 978 product · 10 package
Package marketed since
Apr 18, 2019
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 4125097810 8
FDA record last changed
Oct 1, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41250-978-10
Product NDC 41250-978
11-digit billing NDC 41250097810
RxCUI 476549
UNII H0G9379FGK, NBZ3QY004S
Application # M001
SPL Set ID 376665cc-0a2f-4ff7-91bb-be7e476af7a7
Established class (EPC) Blood Coagulation Factor; Calculi Dissolution Agent; Cations; Inhi
Physiologic effect Increased Coagulation Factor Activity; Increased Large Intestinal Motility; Inhibition Large Intestine Fluid/Electrolyte Absorption
Chemical class Calcium; Divalent
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-04-18
Route ORAL
Dosage form TABLET, CHEWABLE
Substance CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
Quick answers
  • RxCUI (RxNorm): 476549
Why two NDCs? The FDA registers this code as 41250-978-10 — 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 → 41250-0978-10. 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.

RxNorm drug class

This medicine belongs to the Calcium compounds class.

Drug family (ATC) Calcium compounds, Calcium
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📖 About the active ingredient: Calcium Carbonate; Magnesium Hydroxide MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Read the full MedlinePlus article ↗
🧪 What is this product?

Meijer Extra Strength Freshmint Flavor is a chewable tablet antacid containing calcium carbonate and magnesium hydroxide. This is an over-the-counter monograph product, meaning it is marketed under the FDA's established category rules rather than as an individually reviewed application. Calcium carbonate and magnesium hydroxide are both bases that are typically used to neutralize stomach acid and relieve heartburn, acid indigestion, and upset stomach. The tablet is meant to be chewed by mouth.

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
41250-0978-10 You're viewing this Main listing 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC 2019-04-18 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Rolaids Extra Strength Mint 675 mg/1; 135 mg 41167-1001-00 Chattem, 120 tablets — — Discontinued —
Rolaids Extra Strength Fruit 675 mg/1; 135 mg 41167-1002-00 Chattem, 120 tablets — — Discontinued —
Meijer Extra Strength Freshmint Flavor 675 mg/1; 135 mgthis 41250-0978-10 MEIJER 100 tablets — — FDA listed —
Extra Strength Antacid Freshmint 675 mg/1; 135 mg 53943-0108-10 DISCOUNT 100 tablets — — FDA listed —
Best Choice Extra Strength 675 mg/1; 135 mg 63941-0071-10 BEST 100 tablets — — FDA listed —
Premier Value Extra Strength Freshmint Flavor 675 mg/1; 135 mg 68016-0678-00 CHAIN 100 tablets — — FDA listed —
Rolaids Extra Strength Antacid Mint 675 mg/1; 135 mg 69423-0827-03 THE 10 tablets — — FDA listed —
Rolaids ORIGINAL 675 mg/1; 135 mg 84126-0324-03 THE 10 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 White
ShapeRound
ImprintRP107
Size16 mm
ScoringNot scored
FlavorMint
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 IY9XDZ35W2
    Dextrose is a simple sugar derived from corn or other sources. It serves as a filler and sweetener in medicines to add bulk, improve taste, and help stabilize the medication's form.
  • 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 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • 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.

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

The official label also statescorn starch, dextrose, flavor, magnesium stearate, maltodextrin, 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
FDA applicationM001 (OTC MONOGRAPH DRUG)
Labeler code41250
First marketedApr 2019
Product typeHuman Otc Drug
Portfolio245 products on file

More NDCs from MEIJER DISTRIBUTION INC labeler code 41250

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Ask a Doctor or Pharmacist Before Use If 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 7 words ▾

Uses relieves: heartburn sour stomach acid indigestion

⏱️ Dosage and Administration 19 words ▾

Directions chew 2-4 tablets completely as symptoms occur or as directed by a doctor. Do not swallow tablets whole.

⚠️ Warnings 55 words ▾

Warnings Ask a doctor or pharmacist before use if you are now taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product do not take more than 10 tablets in a 24-hour period, do not use the maximum dosage for more than 2 weeks Keep out of reach of children.

🧪 Active Ingredient 15 words ▾

Active ingredients (in each tablet) Calcium Carbonate USP 675 mg Magnesium hydroxide USP 135 mg

🧪 Inactive Ingredients 12 words ▾

Inactive ingredients corn starch, dextrose, flavor, magnesium stearate, maltodextrin, sucralose. Questions? 1-866-467-2748

🎯 Purpose 3 words ▾

Purpose Antacid Antacid

📄 Ask a Doctor or Pharmacist Before Use If 48 words ▾

Ask a doctor or pharmacist before use if you are now taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product do not take more than 10 tablets in a 24-hour period, do not use the maximum dosage for more than 2 weeks

📄 When Using This Product 26 words ▾

When using this product do not take more than 10 tablets in a 24-hour period, do not use the maximum dosage for more than 2 weeks

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Questions or Comments 2 words ▾

Questions? 1-866-467-2748

📄 Package Label / Principal Display Panel 96 words ▾

PRINCIPAL DISPLAY PANEL Meijer ® NDC# 41250-978-10 Compare to Rolaids® Extra Strength active ingredients* Antacid Tablets Calcium Carbonate USP 675 mg Magnesium Hydroxide USP 135 mg Extra Strength Freshmint Flavor Naturally and Artificially Flavored Relieves: Heartburn, Acid Indigestion 100 CHEWABLE TABLETS GLUTEN FREE K PAREVE OUR QUALITY GURANTEE WWW.MEIJER.COM/SATISFACTION TAMPER EVIDENT: DO NOT USE IF PRINTED INNER SEAL IS BROKEN OR MISSING *This product is not manufactured or distributed by Chattem Inc., owner of the registered trademark Rolaids ® DIST.

BY MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544 www.meijer.com antacid tablets calcium carbonate and magnesium hydroxide

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
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 "Otc Monograph Drug". 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.
← 41250-0976-68 · Meijer, 41250-0979-02 · 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.