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Rolaids Advanced Antacid Anti-gas Wild Berry Calcium carbonate and Magnesium hydroxide and Simethicone 1000 mg; 200 mg; 40 mg Tablet, Chewable, 60-count — NDC 41167-1041-0 (Billing 41167-1041-00)

by Chattem, Inc. · 60 TABLET, CHEWABLE in 1 BOTTLE

This is a package of 60 tablets of Rolaids Advanced Antacid Anti-gas Wild Berry Calcium carbonate and Magnesium hydroxide and Simethicone 1000 mg; 200 mg; 40 mg Tablet, Chewable from Chattem, Inc., marketed since Feb 2023 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 41167-1041-00
🏷️ FDA NDC (as labeled) 41167-1041-0 billing pads the package segment with a zero
This package
Contains60-count Pack sizes3 compare ↓
Main listing for product 41167-1041 · Also comes in: 10 tablets 41167-1041-1 10 tablets 41167-1041-2
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 41167-1041-0 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
41167 labeler · 1041 product · 0 package
Package marketed since
Feb 1, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0041167104057
FDA record last changed
Oct 1, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41167-1041-0
Product NDC 41167-1041
11-digit billing NDC 41167104100
RxCUI 1649510
UNII H0G9379FGK, NBZ3QY004S, 92RU3N3Y1O
UPC 0041167104057
Application # M001
SPL Set ID 07649a83-0123-4bb5-b130-3067c7d052c5
Physiologic effect Skin Barrier Activity
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-02-01
Route ORAL
Dosage form TABLET, CHEWABLE
Substance CALCIUM CARBONATE; MAGNESIUM HYDROXIDE; DIMETHICONE
Quick answers
  • RxCUI (RxNorm): 1649510
Why two NDCs? The FDA registers this code as 41167-1041-0 — 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 → 41167-1041-00. 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

🧪 What is this product?

Rolaids Advanced Antacid Anti-gas is a chewable tablet taken by mouth that contains three active ingredients commonly used to manage heartburn and gas discomfort. Calcium carbonate and magnesium hydroxide are antacids that work by neutralizing stomach acid, while dimethicone (also called simethicone) is a defoaming agent typically used to help reduce gas bubbles in the stomach and intestines. This product is an over-the-counter monograph drug, meaning it is marketed under FDA's established rules for antacid and anti-gas products.

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.
Try another pack size: 10 tablets 10 tablets
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
41167-1041-00 You're viewing this Main listing 60 TABLET, CHEWABLE in 1 BOTTLE 2023-02-01 — Active
41167-1041-01 41167-1041-1 10 TABLET, CHEWABLE in 1 CELLO PACK 2023-02-01 — Active
41167-1041-02 41167-1041-2 3 CELLO PACK in 1 PACKAGE / 10 TABLET, CHEWABLE in 1 CELLO PACK 2023-02-01 — Active

Pack size FAQ

What quantity is in this package?
This is a 60-count package — 60 tablet, chewable in 1 bottle.
How does this package differ from NDC 41167-1041-01?
Both are Rolaids Advanced Antacid Anti-gas Wild Berry Calcium carbonate and Magnesium hydroxide and Simethicone 1000 mg; 200 mg; 40 mg Tablet, Chewable — the drug itself is identical. This page's package is the 60-count one, while NDC 41167-1041-01 is the 10 tablets package.
What NDC number is used to bill for this package of Rolaids Advanced Antacid Anti-gas Wild Berry Calcium carbonate and Magnesium hydroxide and Simethicone 1000 mg; 200 mg; 40 mg Tablet, Chewable?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Rolaids Advanced Antacid Anti-gas Mixed Berry 1000 mg/1; 200 mg/1; 40 mg 41167-1040-00 Chattem, 75 tablets — — Discontinued —
Rolaids Advanced Antacid Anti-gas Wild Berry 1000 mg/1; 200 mg/1; 40 mgthis 41167-1041-00 Chattem, 60 tablets — — FDA listed —
Rolaids Multi-Symptom Advanced Antacid plus Anti-gas Wild Berry 1000 mg/1; 200 mg/1; 40 mg 69423-0826-01 THE 10 tablets — — FDA listed —
Rolaids Heartburn plus Gas 40 mg/1; 1000 mg/1; 200 mg 84126-0343-01 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

🏛️
2023
On the market since
Feb 2023
📍
2026
Currently FDA-listed
3 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 pink / blue / purple / red
ShapeRound
ImprintR;A
Size19 mm
ScoringNot scored
FlavorBlueberry
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.

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

LabelerChattem, Inc.
FDA applicationM001 (OTC MONOGRAPH DRUG)
Labeler code41167
First marketedFeb 2023
Product typeHuman Otc Drug
Portfolio157 products on file

More NDCs from Chattem, Inc. labeler code 41167

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 33 words ▾

Uses for the relief of: ■ heartburn ■ sour stomach ■ acid indigestion ■ upset stomach associated with these symptoms ■ pressure and bloating, commonly referred to as gas, associated with these symptoms

⏱️ Dosage and Administration 14 words ▾

Directions ■ chew 2-3 tablets as symptoms occur, or as directed by a doctor

⚠️ Warnings 57 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 7 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 19 words ▾

Active ingredients (in each tablet) Calcium carbonate USP 1000 mg Magnesium hydroxide USP 200 mg Simethicone USP 40 mg

🧪 Inactive Ingredients 31 words ▾

Inactive ingredients corn starch, dextrose, FD&C blue no. 1 lake, FD&C red no. 40 lake, magnesium stearate, maltodextrin, natural and artificial flavor, propylene glycol alginate, silicon dioxide, stearic acid, sucrose, triacetin

🎯 Purpose 4 words ▾

Purposes Antacid Antacid Antigas

📄 Ask a Doctor or Pharmacist Before Use If 22 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 28 words ▾

When using this product ■ do not take more than 7 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 18 words ▾

Questions ? Call 1- 866-844-2798 or visit www. ROLAIDS .com Keep carton as it contains important product information.

📄 Package Label / Principal Display Panel 51 words ▾

PRINCIPAL DISPLAY PANEL MULTI-SYMPTOM Rolaids ® ADVANCED ANTACID + ANTI-GAS 10 Chewable Tablets Wild Berry Rolaids® ADVANCED ANTACID + ANTI-GAS 10 Chewable Tablets Wild Berry

PRINCIPAL DISPLAY PANEL MULTI-SYMPTOM Rolaids ® ADVANCED ANTACID + ANTI-GAS 60 Chewable Tablets Wild Berry MULTI-SYMPTOM Rolaids® ADVANCED ANTACID + ANTI-GAS 60 Chewable Tablets Wild Berry

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 — 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 "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 Chattem, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 10 tablets (41167-1041-01), 10 tablets (41167-1041-02). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Chattem, 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.
← 41167-1040-00 · Chattem, 41167-1651-04 · Chattem, →
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.