Stomach Relief
- Product NDC
- 17856-8286
- 11-digit product format
- 178568286
- Labeler code
- 17856
- Product ID
- 17856-8286_401f8cd0-5b2a-d6b0-e063-6394a90ad8e8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corp
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-03-29
- 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
- Stomach Relief
- Brand name suffix
- Regular Strength
- 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 |
|---|
| 17856-8286-1 | Stomach ReliefRegular Strength | 50 in 1 CASE | LIQUID | 50 | | 1 |
| 17856-8286-1 | Stomach ReliefRegular Strength | 15 mL in 1 CUP, UNIT-DOSE | LIQUID | 15 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 17856-8286-1 | 17856828601 | 50 CUP, UNIT-DOSE in 1 CASE (17856-8286-1) / 15 mL in 1 CUP, UNIT-DOSE | 2025-10-01 | No | No | Current |