Indications and uses
relieves: heartburn sour stomach acid indigestion
Rolaids Extra Strength Tablets Mint
- Manufacturer
- THE PROCTER & GAMBLE MANUFACTURING COMPANY
- Effective date
- 2026-10-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- daily-update
- Hydrated at
- 2026-10-06 02:01:56
Label at a glance#
ProductRolaids Extra Strength Antacid Mint
Active ingredientCALCIUM CARBONATE, MAGNESIUM HYDROXIDE
Label structure11 sections
Dosage and administration
chew 2-4 tablets as symptoms occur, or as directed by a doctor
Label contents#
Full prescribing information#
Rolaids Extra Strength Mint
Drug Facts
Active ingredient (in each tablet)
Calcium carbonate USP 675 mg
Magnesium hydroxide USP 135 mg
Purpose
Antacid
Antacid
Uses
relieves:
- heartburn
- sour stomach
- acid indigestion
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.
Directions
- chew 2-4 tablets as symptoms occur, or as directed by a doctor
Other information
each tablet contains:calcium 270 mg, magnesium 55mg
Inactive ingredients
dextrose, flavor, magnesium stearate, maltodextrin, silicon dioxide, stearic acid, sucralose, sucrose
Tamper Evident
Do not use if inner foil seal on bottle is broken or missing.
SPL UNCLASSIFIED SECTION
DIST. BY: PROCTER &
GAMBLE, CINCINNATI, OH
45202
PRINCIPAL DISPLAY PANEL
EXTRASTRENGTH ANTACID
Rolaids
®
ANTACID
GOES TO WORK INSTANTLY
Mint Naturally & Artificially Flavored
96 Chewable Tablets
DailyMed Product Concepts#
Products#
Every source-derived product name is available through these pages.
- Rolaids Extra Strength Antacid Mint
- Calcium carbonate and Magnesium hydroxide
- CALCIUM CARBONATE
- CALCIUM CATION
- MAGNESIUM HYDROXIDE
- MAGNESIUM CATION
- DEXTROSE
- MAGNESIUM STEARATE
- SILICON DIOXIDE
- STEARIC ACID
- SUCRALOSE
- SUCROSE
- MALTODEXTRIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69423-827 | 69423-827-01, 69423-827-03, 69423-827-96 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CALCIUM CARBONATE | H0G9379FGK | ACTIB |
| MAGNESIUM HYDROXIDE | NBZ3QY004S | ACTIB |
| DEXTROSE | IY9XDZ35W2 | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| SUCROSE | C151H8M554 | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 5 | 2025-10-03 | full-release | 2026-06-01 01:15:43 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 404124bd-3b55-a3a7-e063-6294a90a9cf9 | 0ce3e7ee-aa52-16bc-e063-6294a90a527d | 2025-10-03 | Warnings | 0ce3e7ee-aa52-16bc-e063-6294a90a527d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.