up and up 5-symptom digestive relief
- Product NDC
- 11673-125
- 11-digit product format
- 116730125
- Labeler code
- 11673
- Product ID
- 11673-125_42c36460-f332-0c52-e063-6394a90af168
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-09-07
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 262 mg/1
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- up and up 5-symptom digestive relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 262 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 308760 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11673-125-20 | up and up 5-symptom digestive relief | 40 in 1 BOTTLE, PLASTIC | TABLET | 40 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-125 | UP AND UP 5-SYMPTOM DIGESTIVE RELIEF (BISMUTH SUBSALICYLATE) TABLET [TARGET CORPORATION] | 8 | Current NDC, Legacy NDC, 1 package rows | 20241109_6462e224-5ee7-4556-90f2-994eaf89b71b.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 |
|---|
| 11673-125-20 | 11673012520 | 40 TABLET in 1 BOTTLE, PLASTIC (11673-125-20) | 40 tablet | 2015-09-07 | 0000-00-00 | No | No | Current |