Bismuth Subsalicylate
- Product NDC
- 81033-046
- Requested package NDC
- 81033-046-34
- 11-digit product format
- 810330046
- Labeler code
- 81033
- Product ID
- 81033-046_5b126fca-aaea-4d57-e063-6394a90aafb5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Kesin Pharma
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-02-03
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/30mL
- 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.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bismuth Subsalicylate
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BISMUTH SUBSALICYLATE | 525 mg/30mL |
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 | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 81033-046-34 | 81033004634 | 30 CUP, UNIT-DOSE in 1 CARTON (81033-046-34) / 15 mL in 1 CUP, UNIT-DOSE (81033-046-15) | 2026-09-09 | No | No | Current |