Pepto Bismol
- Product NDC
- 69423-966
- 11-digit product format
- 694230966
- Labeler code
- 69423
- Product ID
- 69423-966_47f5d3d6-3794-6bb2-e063-6294a90a42e6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-03-07
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/15mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pepto Bismol
- Brand name suffix
- Ultra
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 525 mg/15mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 211915, 308763 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69423-966-12 | Pepto BismolUltra | 354 mL in 1 BOTTLE, PLASTIC | SUSPENSION | 354 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69423-966 | PEPTO BISMOL ULTRA (BISMUTH SUBSALICYLATE) SUSPENSION [THE PROCTER & GAMBLE MANUFACTURING COMPANY] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241012_d800eb8c-42c8-fb12-e053-2a95a90af2a2.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 |
|---|
| 69423-966-12 | 69423096612 | 354 mL in 1 BOTTLE, PLASTIC (69423-966-12) | 354 ml | 2022-03-07 | 0000-00-00 | No | No | Current |