Mucus Relief
- Product NDC
- 11822-0731
- 11-digit product format
- 118220731
- Labeler code
- 11822
- Product ID
- 11822-0731_f9438448-b525-47e4-82ac-40f2d4e170cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2019-05-31
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 11822-0731 | MUCUS RELIEF (GUAIFENESIN) TABLET [RITE AID CORPORATION] | 3 | Legacy NDC | 20230221_b091ace8-72ab-426a-bba6-97787805f63e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0731-1 | 11822073101 | 100 BLISTER PACK in 1 CARTON (11822-0731-1) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2019-05-31 | 0000-00-00 | No | No | Current |
| 11822-0731-6 | 11822073106 | 68 BLISTER PACK in 1 CARTON (11822-0731-6) > 1 TABLET in 1 BLISTER PACK | 68 blister pack | 2019-05-31 | 0000-00-00 | No | No | Current |