Digestive Relief
- Product NDC
- 21130-125
- 11-digit product format
- 211300125
- Labeler code
- 21130
- Product ID
- 21130-125_424aa911-6748-010b-e063-6394a90a7ae7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth Subsalicylate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- SAFEWAY
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-10-05
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 262 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
- 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 |
|---|
| 21130-125-40 | Digestive Relief | 40 in 1 BOTTLE | TABLET, FILM COATED | 40 | | 6 |
| 21130-125-40 | Digestive Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-125 | DIGESTIVE RELIEF (BISMUTH SUBSALICYLATE) TABLET, FILM COATED [SAFEWAY] | 5 | Current NDC, Legacy NDC, 2 package rows | 20241105_5538d56a-b258-4260-b51b-f5131bd76885.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 |
|---|
| 21130-125-40 | 21130012540 | 1 BOTTLE in 1 CARTON (21130-125-40) / 40 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-10-05 | 0000-00-00 | No | No | Current |