Bismuth
- Product NDC
- 55910-682
- 11-digit product format
- 559100682
- Labeler code
- 55910
- Product ID
- 55910-682_8f50f78e-95ee-4f10-8512-37340f1f9f53
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
- Application
- part335
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-07-31
- Marketing end
- 2024-04-12
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 1050 mg/30mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55910-682-12 | 55910068212 | 354 mL in 1 BOTTLE, PLASTIC (55910-682-12) | 354 ml | 2018-07-31 | 2024-04-12 | No | No | Current |