Dosage and administration
adults and children 12 years of age and over: chew 2-4 tablets as symtoms occur, or as directed by a doctor do not take for symtoms that persist for more than 2 weeks unless advised by a doctor
adults and children 12 years of age and over: chew 2-4 tablets as symtoms occur, or as directed by a doctor do not take for symtoms that persist for more than 2 weeks unless advised by a doctor
Calcium Carbonate 500mg
Antacid
Relieves • acid indigestion • heartburn • sour stomach • upset stomach associated with these symptoms
Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
When using this product
Keep out of of reach of children
D&C Yellow No.10 lake, FD&C Blue No.1 lake, flavor, magnesium stearate, sorbitol, sucralose.
1-888-309-9030
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71481-011-01 | 2025-01-30 | C162847 | 48780-1 | 1030e365-2d8d-111a-e063-dadaa90a10e2 | 8ac97273-58f6-401e-94c9-c6d3cc3da68b |
| 71481-011-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-2d8d-111a-e063-dadaa90a10e2 | 8ac97273-58f6-401e-94c9-c6d3cc3da68b |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71481-011-01 | DGH Antacid Peppermint 500,150ct | 150 in 1 BOTTLE | TABLET, CHEWABLE | 150 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 71481-011 | 71481-011-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| D&C YELLOW NO. 10 ALUMINUM LAKE | CQ3XH3DET6 | IACT |
| FD&C BLUE NO. 1 ALUMINUM LAKE | J9EQA3S2JM | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| SORBITOL | 506T60A25R | IACT |
| 5-METHYL-1,3,5-TRIPHENYL-2-PYRAZOLINE | 96K6O83026 | IACT |
| CALCIUM CARBONATE | H0G9379FGK | ACTIB |
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 |
|---|---|---|---|---|---|---|
| f6421850-a0ff-d275-e053-2a95a90a544a | 8ac97273-58f6-401e-94c9-c6d3cc3da68b | 2023-03-06 | Warnings | f6421850-a0ff-d275-e053-2a95a90a544a 8ac97273-58f6-401e-94c9-c6d3cc3da68b |
Adverse event summaries are temporarily unavailable. Other product information remains available.