PUBLIX Stomach Relief
- Product NDC
- 41415-707
- 11-digit product format
- 414150707
- Labeler code
- 41415
- Product ID
- 41415-707_42375f33-2648-bfb8-e063-6394a90a6501
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- PUBLIX SUPER MARKETS, INC
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-10-24
- 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
- PUBLIX Stomach Relief
- Brand name suffix
- Ultra Strength
- 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 |
|---|
| 41415-707-12 | PUBLIX Stomach ReliefUltra Strength | 354 mL in 1 BOTTLE | SUSPENSION | 354 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41415-707 | PUBLIX STOMACH RELIEF ULTRA STRENGTH (BISMUTH SUBSALICYLATE) SUSPENSION [PUBLIX SUPER MARKETS, INC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241030_4be86e84-fddf-4eb5-a519-64009d0e69fc.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 |
|---|
| 41415-707-12 | 41415070712 | 354 mL in 1 BOTTLE (41415-707-12) | 354 ml | 2022-10-24 | 0000-00-00 | No | No | Current |