Antacid Anti-Gas Relief Chews
- Product NDC
- 55319-018
- Requested package NDC
- 55319-018-32
- 11-digit product format
- 553190018
- Labeler code
- 55319
- Product ID
- 55319-018_ecfa0b1a-e2b0-0371-e053-2a95a90a16b0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium Carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Family Dollar
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-01-26
- Marketing end
- 0000-00-00
- Substance
- CALCIUM CARBONATE; DIMETHICONE
- Active strength
- 750 mg/1; mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Skin Barrier Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 55319-018 | 55319-018-32 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 55319-018-32 | 55319001832 | 32 TABLET, CHEWABLE in 1 BOTTLE (55319-018-32) | 2018-01-26 | 0000-00-00 | No | No | Current |