Bismuth Subsalicylate 262 mg
- Product NDC
- 69618-029
- 11-digit product format
- 696180029
- Labeler code
- 69618
- Product ID
- 69618-029_2bc8473d-ad00-da1d-e063-6394a90ae0d4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth Subsalicylate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Reliable 1 Laboratories LLC
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-11-01
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 262 mg/1
- 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
- Bismuth Subsalicylate 262 mg
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 262 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 308761 |
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 |
|---|
| 69618-029-03 | Bismuth Subsalicylate 262 mg | 30 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69618-029 | BISMUTH SUBSALICYLATE 262 MG (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [RELIABLE 1 LABORATORIES LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250117_2e40ffd8-1afa-43af-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69618-029-03 | 69618002903 | 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (69618-029-03) | 2015-11-01 | 0000-00-00 | No | No | Current |