BestHealth Orange Antacid Soft Chews
- Manufacturer
- Bestco LLC
- Effective date
- 2022-11-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:47:30
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient (in each chew)
Calcium Carbonate 1177 mg
OTC - PURPOSE SECTION
Purpose
Antacid
INDICATIONS & USAGE SECTION
Uses Relieves
- heartburn
- sour stomach
- acid indigestion
- upset stomach associated with these symptoms
WARNINGS SECTION
Warnings
Ask a doctor or pharmacist before use if you are now taking a prescription drug. Antacids may interact with certain prescription drugs.
OTC - WHEN USING SECTION
When using this product do not take more than 6 chews in a 24-hour period, or use the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If you are pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
DOSAGE & ADMINISTRATION SECTION
Directions
Chew and swallow 2 to 3 chews, as symptoms occur or as directed by a physician.
OTHER SAFETY INFORMATION
Other information
- Each chew contains: calcium 470 mg, magnesium 5 mg
- Contains milk and soy
- Store between 20° to 25°C (68° to 77°F) in a dry place
- Do not use if bag is torn or open
INACTIVE INGREDIENT SECTION
Inactive ingredients: Confectioner's sugar, corn starch, corn syrup, corn syrup solids, FD&C yellow #6 aluminum lake, glycerin, hydrogenated coconut oil, natural and artificial flavors, nonfat dry milk, soy lecithin, sucrose.
OTC - QUESTIONS SECTION
Questions? Or to report an adverse event call 1-800-245-2898, Monday - Friday, 9AM to 4PM EST
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- BestHealth Orange Antacid Soft Chews
- Calcium Carbonate
- CALCIUM CATION
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 52642-048 | 52642-048-32 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CALCIUM CARBONATE | H0G9379FGK | ACTIB |
| SUCROSE | C151H8M554 | 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 |
|---|---|---|---|---|---|---|
| 0982680c-cb6c-55af-e063-6394a90a32d3 | 9b7bfd08-fd91-5b38-e053-2a95a90ab51a | 2023-11-06 | Warnings | 9b7bfd08-fd91-5b38-e053-2a95a90ab51a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
