Select Brand Mucus Relief
- Product NDC
- 15127-171
- 11-digit product format
- 151270171
- Labeler code
- 15127
- Product ID
- 15127-171_4ce95bba-0bd7-4ee0-96c2-9d9887ec445c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin/phenylephrine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Select Brand Distributors
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2006-06-05
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 400 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 15127-171-50 | Select Brand Mucus Relief PE | 1 in 1 CARTON | TABLET | 1 | | 1 |
| 15127-171-50 | Select Brand Mucus Relief PE | 50 in 1 BOTTLE | TABLET | 50 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 15127-171 | SELECT BRAND MUCUS RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [SELECT BRAND DISTRIBUTORS] | 1 | Legacy NDC, 2 package rows | 20140926_ab7ca98a-e6ca-4f91-a199-e69b9c86b4e2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 15127-171-50 | 15127017150 | 1 in 1 CARTON | Historical |