Rite Aid Digestive Relief
- Product NDC
- 11822-1254
- 11-digit product format
- 118221254
- Labeler code
- 11822
- Product ID
- 11822-1254_71b12479-5c18-49f3-8c4c-5b5afbd333d8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth Subsalicylate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RITE AID CORPORATION
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-03-31
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 262 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 11822-1254_71b12479-5c18-49f3-8c4c-5b5afbd333d8
- Product type
- HUMAN OTC DRUG
- Finished product
- Yes
- Brand name base
- Rite Aid Digestive Relief
- Generic name
- Bismuth Subsalicylate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing start
- 2020-03-31
- Marketing category
- OTC MONOGRAPH DRUG
- Application number
- M008
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 262 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 308760 |
| Spl Set Id | 816c4ec4-46d1-4e8e-ad91-a11946c48769 |
| Manufacturer Name | RITE AID CORPORATION |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 62TEY51RR1 | BISMUTH SUBSALICYLATE | 14882-18-9 | BISMUTH SUBSALICYLATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-1254-0 | 11822125400 | 1 BOTTLE in 1 CARTON (11822-1254-0) / 40 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-03-31 | 0000-00-00 | No | No | Current |