Stomach Relief, Ultra Strength
- Product NDC
- 68998-558
- 11-digit product format
- 689980558
- Labeler code
- 68998
- Product ID
- 68998-558_182ef664-b0b4-47c0-9453-27bc5d80d0f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BISMUTH SUBSALICYLATE
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Marc Glassman, Inc.
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-12-15
- 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
- Stomach Relief, Ultra Strength
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68998-558-28 | Stomach Relief, Ultra Strength | 354 mL in 1 BOTTLE | SUSPENSION | 354 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68998-558 | STOMACH RELIEF, ULTRA STRENGTH (BISMUTH SUBSALICYLATE) SUSPENSION [MARC GLASSMAN, INC.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20201220_8e47d007-237c-45c7-88c5-83953a06e4bd.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 |
|---|
| 68998-558-28 | 68998055828 | 354 mL in 1 BOTTLE (68998-558-28) | 354 ml | 2020-12-15 | 0000-00-00 | No | No | Current |