Mucus Relief
- Product NDC
- 11822-2252
- 11-digit product format
- 118222252
- Labeler code
- 11822
- Product ID
- 11822-2252_293140d0-c8f2-4fe2-9672-5fa544458a4c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2019-12-27
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-2252 | MUCUS RELIEF (GUAIFENESIN) TABLET [RITE AID CORPORATION] | 3 | Legacy NDC | 20230221_c92f809d-cd0a-4f24-908c-6c1403a3b2b7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-2252-7 | 11822225207 | 20 BLISTER PACK in 1 CARTON (11822-2252-7) > 1 TABLET in 1 BLISTER PACK | 20 blister pack | 2019-12-27 | 0000-00-00 | No | No | Current |