Select Brand Mucus Relief
- Product NDC
- 15127-129
- 11-digit product format
- 151270129
- Labeler code
- 15127
- Product ID
- 15127-129_6bf19556-aebc-4a05-bd55-0a59254e92dc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Select Brand Distributors
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-09-26
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 200 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 |
|---|
| 15127-129-60 | Select Brand Mucus Relief | 1 in 1 BOTTLE | TABLET | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 15127-129 | SELECT BRAND MUCUS RELIEF (GUAIFENESIN) TABLET [SELECT BRAND DISTRIBUTORS ] | 1 | Legacy NDC, 1 package rows | 20140929_677ef456-bfa3-4dbd-b39a-1f2b939351d0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 15127-129-60 | 15127012960 | 1 in 1 BOTTLE | Historical |