QUALITY CHOICE
- Product NDC
- 83324-337
- 11-digit product format
- 833240337
- Labeler code
- 83324
- Product ID
- 83324-337_3e89e0f5-7186-ed0b-e063-6294a90ab2b1
- 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
- 2025-07-07
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/15mL
- 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
- QUALITY CHOICE
- Brand name suffix
- ULTRA STRENGTH STOMACH RELIEF
- Listing expiration
- 2026-12-31
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 |
|---|
| 83324-337-08 | QUALITY CHOICEULTRA STRENGTH STOMACH RELIEF | 236 mL in 1 BOTTLE, PLASTIC | LIQUID | 236 | | 2 |
| 83324-337-12 | QUALITY CHOICEULTRA STRENGTH STOMACH RELIEF | 354 mL in 1 BOTTLE, PLASTIC | LIQUID | 354 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83324-337-08 | 83324033708 | 236 mL in 1 BOTTLE, PLASTIC (83324-337-08) | 236 ml | 2025-07-07 | No | No | Historical |
| 83324-337-12 | 83324033712 | 354 mL in 1 BOTTLE, PLASTIC (83324-337-12) | 354 ml | 2025-08-22 | No | No | Historical |