Stomach Relief
- Product NDC
- 41520-372
- Requested package NDC
- 41520-372-12
- 11-digit product format
- 415200372
- Labeler code
- 41520
- Product ID
- 41520-372_32c4da6b-afec-4833-bbc7-dabfa0320f44
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Care One (American Sales Company)
- Application
- part335
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-09-30
- Marketing end
- 0000-00-00
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/30mL
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- 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 | 41520-372 | 41520-372-12 | D | Discontinued by firm | 2026-10-05 |
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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41520-372-12 | 41520037212 | 355 mL in 1 BOTTLE, PLASTIC (41520-372-12) | 355 ml | 2018-09-30 | 0000-00-00 | No | No | Current |