STOMACH RELIEF
- Product NDC
- 37835-207
- 11-digit product format
- 378350207
- Labeler code
- 37835
- Product ID
- 37835-207_5c3a304d-f484-a826-e063-6294a90ab3e1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bi-Mart
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-01
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 262 mg/1
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 37835-207-48 | 37835020748 | 4 BLISTER PACK in 1 BOX (37835-207-48) / 12 TABLET in 1 BLISTER PACK | 4 blister pack | 2025-06-01 | No | No | Historical |