Stomach Relief
- Product NDC
- 63868-832
- Requested package NDC
- 63868-832-08
- 11-digit product format
- 638680832
- Labeler code
- 63868
- Product ID
- 63868-832_31d77f43-2f04-436c-968f-24a4b9a8d934
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- part335
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-03-26
- Marketing end
- 0000-00-00
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/30mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-832 | STOMACH RELIEF (BISMUTH SUBSALICYLATE) LIQUID [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)] | 3 | Legacy NDC | 20241102_4db6aec7-48ab-40b5-9060-7a1a166bdebf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63868-832-08 | 63868083208 | 237 mL in 1 BOTTLE, PLASTIC (63868-832-08) | 237 ml | 2021-03-26 | 0000-00-00 | No | No | Current |