Stomach Relief
- Product NDC
- 63868-813
- 11-digit product format
- 638680813
- Labeler code
- 63868
- Product ID
- 63868-813_a9a6cd23-d557-4dad-b813-4a8662eee2e6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-06-25
- Marketing end
- 2026-06-25
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/15mL
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Stomach Relief
- Brand name suffix
- Ultra Strength
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 525 mg/15mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 308763 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63868-813-08 | Stomach ReliefUltra Strength | 237 mL in 1 BOTTLE, PLASTIC | LIQUID | 237 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-813 | STOMACH RELIEF ULTRA STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241102_b8bcdbb3-9210-4bf6-9ef2-1ed8e3ec255d.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 |
|---|
| 63868-813-08 | 63868081308 | 237 mL in 1 BOTTLE, PLASTIC (63868-813-08) | 237 ml | 2021-06-25 | 2026-06-25 | No | No | Current |