ULTRA STRENGHT PINK BISMUTH
- Product NDC
- 11673-907
- 11-digit product format
- 116730907
- Labeler code
- 11673
- Product ID
- 11673-907_42d687a3-14af-be78-e063-6394a90a396b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- TARGET CORPORATION
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-10-15
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/15mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ULTRA STRENGHT PINK BISMUTH
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 525 mg/15mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 308763 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11673-907-08 | ULTRA STRENGHT PINK BISMUTH | 236 mL in 1 BOTTLE | SUSPENSION | 236 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-907 | ULTRA STRENGHT PINK BISMUTH (BISMUTH SUBSALICYLATE) SUSPENSION [TARGET CORPORATION] | 7 | Current NDC, Legacy NDC, 1 package rows | 20241109_20063215-f657-487b-9530-6df0181b440a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-907-08 | 11673090708 | 236 mL in 1 BOTTLE (11673-907-08) | 236 ml | 2019-10-15 | 0000-00-00 | No | No | Current |