Orange Antacid Softchew
- Manufacturer
- BestCo Inc.
- Effective date
- 2014-03-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:49:26
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 due to 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 perscription drugs.
Do not take more than 6 chews in a 34-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 ae pregnant or nursing a baby, ask a doctor before using this product.
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, mangesium 5mg
Contains milk and soy
Store between 20° to 25ºC (68º to 77ºF) in a dry place
INACTIVE INGREDIENT SECTION
inactive ingredients: Corn syrup, corn syrup solids, FD&C yellow #6 aluminum lake, glycerin, hydrogenated coconut oil, natural and artificial flavors, non-fat dairy milk powder, soy lecithin, and sucrose. Soybean oil and corn starch used as processing aids.
OTC - QUESTIONS SECTION
Questions? Or to report an adverse event call 1-800-245-2898, Monday - Friday, 8AM -4PM EST
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| CALCIUM CATION Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20230427 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| bee4fa8d-8d82-423a-a0b5-40a89dd13a99 | Product name | 1 | 20250618 |
| e0d2eb29-08bd-4bba-90d1-c91c68a38767 | Product name | 4 | 20250516 |
| 30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2 | Product name | 5 | 20250304 |
| 334fe8d2-68fb-4331-a576-420e302ec069 | Product name | 7 | 20240320 |
| 444b3e50-f226-46ef-bfca-2e7035d140cd | Product name | 1 | 20190611 |
| e92765c1-be81-432a-b909-1b10777ec378 | Product name | 1 | 20190208 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
| 0441a8f5-3835-497c-aedd-bc78cba56b2a | Product name | 1 | 20150317 |
| 87711080-88eb-65c5-b2dd-bf99e700a372 | Product name | 1 | 20140508 |
| ec2149b3-5c6d-5344-f757-c86411073075 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52642-021-32 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-fd9d-f424-e053-dadaa90a57ce | Calcium carbonate 1177 mg |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52642-021-32 | Orange Antacid Softchew | 32 in 1 BAG | TABLET, CHEWABLE | 32 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Orange Antacid Softchew
- Calcium Carbonate
- SUCROSE
- CALCIUM CATION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 52642-021 | 52642-021-32 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| CALCIUM CARBONATE | H0G9379FGK | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 4be28e4b-6cd0-6b26-e054-00144ff8d46c | 4be28e4b-6ccf-6b26-e054-00144ff8d46c | 2014-03-14 | Warnings | 4be28e4b-6cd0-6b26-e054-00144ff8d46c 4be28e4b-6ccf-6b26-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
