Extra Strength Antacid Smooth dissolving - Berry Fusion Flavors
- Manufacturer
- TARGET CORPORATION | TIME CAP LABORATORIES, INC. | MARKSANS PHARMA LIMITED
- Effective date
- 2025-04-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 01:05:54
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
Drug Facts
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active ingredient (Per tablet)
Calcium Carbonate USP 750 mg
OTC - PURPOSE SECTION
Purpose
Antacid
INDICATIONS & USAGE SECTION
Uses relieves
- heartburn
- acid indigestion
- sour stomach
- upset stomach associated with these symptoms
WARNINGS SECTION
Warnings
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
OTC - WHEN USING SECTION
When using this product
- do not take more than 10 tablets in 24 hours
- if pregnant do not take more than 6 tablets in 24 hours
- do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
DOSAGE & ADMINISTRATION SECTION
Directions
- adults and children 12 years of age and over: chew 2 – 4 tablets as symptoms occur, or as directed by a doctor
- do not take for symptoms that persist for more than 2 weeks unless advised by a doctor
OTHER SAFETY INFORMATION
Other information
- each tablet contains : elemental calcium 300 mg, magnesium 9 mg
- store at room temperature.
INACTIVE INGREDIENT SECTION
Inactive ingredients adipic acid, colloidal silicon dioxide, corn starch, dextrose monohydrate, D&C red 27, FD&C blue no. 1 al. lake, FD&C red 40 al. lake, flavors, guar gum, magnesium stearate, maltodextrin, sorbitol, sucralose
OTC - QUESTIONS SECTION
Questions or comments? Call 1-800-910-6874
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11673-568-06 | Extra Strength Antacid Smooth dissolving - Berry Fusion Flavors | 60 in 1 BOTTLE | TABLET, CHEWABLE | 60 | 2 |
Products#
Every source-derived product name is available through these pages.
- Extra Strength Antacid Smooth dissolving - Berry Fusion Flavors
- Calcium Carbonate
- FD&C BLUE NO. 1 ALUMINUM LAKE
- GUAR GUM
- CALCIUM CATION
- CARBONATE ION
- MAGNESIUM STEARATE
- ADIPIC ACID
- STARCH, CORN
- D&C RED NO. 27
- FD&C RED NO. 40 ALUMINUM LAKE
- MALTODEXTRIN
- SORBITOL
- SUCRALOSE
- SILICON DIOXIDE
- DEXTROSE MONOHYDRATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 11673-568 | 11673-568-06 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FD&C BLUE NO. 1 ALUMINUM LAKE | J9EQA3S2JM | IACT |
| GUAR GUM | E89I1637KE | IACT |
| CALCIUM CARBONATE | H0G9379FGK | ACTIB |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| ADIPIC ACID | 76A0JE0FKJ | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| D&C RED NO. 27 | 2LRS185U6K | IACT |
| FD&C RED NO. 40 ALUMINUM LAKE | 6T47AS764T | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| SORBITOL | 506T60A25R | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| DEXTROSE MONOHYDRATE | LX22YL083G | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| Extra Strength Antacid Smooth dissolving - Berry Fusion Flavors | CALCIUM CARBONATE | TARGET CORPORATION | 28fce33f-c561-1512-e063-6294a90a111c | 2025-04-05 | Warnings | 11673-568-06 11673-568 11673056806 32057a64-7164-6dbc-e063-6394a90a2827 28fce33f-c561-1512-e063-6294a90a111c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
