Peptic Relief
- Product NDC
- 21695-639
- 11-digit product format
- 216950639
- Labeler code
- 21695
- Product ID
- 21695-639_39fd1b7e-fac0-4d6f-8bc2-4af6e880a53d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Peptic Relief
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- part335
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-12-30
- Marketing end
- 0000-00-00
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 262 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 21695-639-30 | Peptic Relief | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-639 | PEPTIC RELIEF TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20120105_39fd1b7e-fac0-4d6f-8bc2-4af6e880a53d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-639-30 | 21695063930 | 30 in 1 BOTTLE | Historical |