up and up digestive relief
- Product NDC
- 11673-706
- 11-digit product format
- 116730706
- Labeler code
- 11673
- Product ID
- 11673-706_42d66c91-c31d-408c-e063-6294a90a9ca9
- 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
- 2018-03-15
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/30mL
- 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 digestive relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 525 mg/30mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 308762 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11673-706-08 | up and up digestive relief | 236 mL in 1 BOTTLE | SUSPENSION | 236 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-706 | UP AND UP DIGESTIVE RELIEF (BISMUTH SUBSALICYLATE) SUSPENSION [TARGET CORPORATION] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241109_5731025d-ffaa-4b31-971f-e58b921e40ed.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 |
|---|
| 11673-706-08 | 11673070608 | 236 mL in 1 BOTTLE (11673-706-08) | 236 ml | 2018-03-15 | 0000-00-00 | No | No | Current |