Mucus Relief
- Product NDC
- 21130-955
- 11-digit product format
- 211300955
- Labeler code
- 21130
- Product ID
- 21130-955_681439ae-3cd8-4c74-8061-44967fced2c7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Better Living Brands, LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2005-12-22
- Marketing end
- 2021-07-30
- Substance
- GUAIFENESIN
- Active strength
- 400 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-955-12 | 21130095512 | 1 BOTTLE in 1 CARTON (21130-955-12) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2005-12-22 | 2021-07-30 | No | No | Current |