Ultra Strength digestive relief
- Product NDC
- 30142-138
- 11-digit product format
- 301420138
- Labeler code
- 30142
- Product ID
- 30142-138_3b873634-dbad-e0bc-e063-6294a90a5f74
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- THE KROGER CO.
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-11-18
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ultra Strength digestive relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 525 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 1998447 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 30142-138-24 | Ultra Strength digestive relief | 1 in 1 CARTON | TABLET | 1 | | 7 |
| 30142-138-24 | Ultra Strength digestive relief | 24 in 1 BOTTLE | TABLET | 24 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 30142-138 | ULTRA STRENGTH DIGESTIVE RELIEF (BISMUTH SUBSALICYLATE) TABLET [THE KROGER CO.] | 6 | Current NDC, Legacy NDC, 2 package rows | 20240731_5e288108-1578-4379-a3d6-44b447187643.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 |
|---|
| 30142-138-24 | 30142013824 | 1 BOTTLE in 1 CARTON (30142-138-24) / 24 TABLET in 1 BOTTLE | 1 bottle | 2019-11-18 | 0000-00-00 | No | No | Current |