up and up 5-symptom digestive relief
- Product NDC
- 11673-122
- 11-digit product format
- 116730122
- Labeler code
- 11673
- Product ID
- 11673-122_42c2f050-6c70-6c79-e063-6394a90ade8f
- 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
- 2019-03-12
- 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 |
|---|
| 11673-122-48 | up and up 5-symptom digestive relief | 48 in 1 BOTTLE, PLASTIC | TABLET | 48 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-122 | UP AND UP 5-SYMPTOM DIGESTIVE RELIEF (BISMUTH SUBSALICYLATE) TABLET [TARGET CORPORATION] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241109_7f6b2960-943d-464c-9ff9-4649a8ab4a4e.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 |
|---|
| 11673-122-48 | 11673012248 | 48 TABLET in 1 BOTTLE, PLASTIC (11673-122-48) | 48 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |