Ultra Bismuth
- Product NDC
- 55910-843
- 11-digit product format
- 559100843
- Labeler code
- 55910
- Product ID
- 55910-843_33932a10-54e5-4685-aef5-5df6e9e7253c
- 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
- 2018-09-30
- Marketing end
- 2024-01-12
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/15mL
- 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 |
|---|
| 55910-843-12 | 55910084312 | 355 mL in 1 BOTTLE, PLASTIC (55910-843-12) | 355 ml | 2018-09-30 | 0000-00-00 | No | No | Current |