Max Strength Stomach Relief
- Product NDC
- 69256-528
- 11-digit product format
- 692560528
- Labeler code
- 69256
- Product ID
- 69256-528_4a79f73d-09e6-4713-8787-8d0c36e654de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Harris Teeter, LLC
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-02-06
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 1050 mg/30mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Max Strength Stomach Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 1050 mg/30mL |
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 |
|---|
| 69256-528-04 | Max Strength Stomach Relief | 236 mL in 1 BOTTLE | LIQUID | 236 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69256-528 | MAX STRENGTH STOMACH RELIEF (BISMUTH SUBSALICYLATE) LIQUID [HARRIS TEETER, LLC] | 2 | Current NDC, 1 package rows | 20250214_2c516139-0a6a-5ba6-e063-6394a90aa14a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69256-528-04 | 69256052804 | 236 mL in 1 BOTTLE (69256-528-04) | 236 ml | 2025-02-06 | No | No | Current |