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 arepresently taking a prescription drug. Antacids may interact with certain prescription drugs.
When using this product
Keep out of of reach of children
each tablet contains: elemental calcium 200 mg.
Store at room temperature. Keep the container tightly closed.
D&C Red No.27*, D&C Yellow No.10*, FD&C Blue No.1*, FD&C Yellow No.6*, flavors, guar gum, hypromellose, magnesium stearate, sorbitol, sucralose. (* lake)
1-888-309-9030
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71481-003-01 | 2025-07-29 | C162847 | 48780-1 | 1030e365-3b8b-111a-e063-dadaa90a10e2 | DGH Antacid Regular Strength 500 (Fruit assorted) |
| 71481-003-01 | 2024-04-04 | C162847 | 48780-1 | 1030e365-3b8b-111a-e063-dadaa90a10e2 | DGH Antacid Regular Strength 500 (Fruit assorted) |
| 71481-003-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-3b8b-111a-e063-dadaa90a10e2 | DGH Antacid Regular Strength 500 (Fruit assorted) |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71481-003-01 | DGH Antacid Regular Strength 500 (Fruit assorted), 150ct | 150 in 1 BOTTLE | TABLET | 150 | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 71481-003 | 71481-003-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| D&C RED NO. 27 | 2LRS185U6K | IACT |
| D&C YELLOW NO. 10 ALUMINUM LAKE | CQ3XH3DET6 | IACT |
| FD&C BLUE NO. 1 ALUMINUM LAKE | J9EQA3S2JM | IACT |
| FD&C YELLOW NO. 6 | H77VEI93A8 | IACT |
| GUAR GUM | E89I1637KE | IACT |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| SORBITOL | 506T60A25R | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | 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 |
|---|---|---|---|---|---|---|
| 1549c8ba-ecf6-2b8a-e063-6394a90ab672 | 3a8adf74-a15d-4ca6-8eba-1a4b2f5d41e0 | 2024-04-04 | Warnings | 1549c8ba-ecf6-2b8a-e063-6394a90ab672 3a8adf74-a15d-4ca6-8eba-1a4b2f5d41e0 |
Adverse event summaries are temporarily unavailable. Other product information remains available.