Mucus Relief
- Product NDC
- 11822-3252
- 11-digit product format
- 118223252
- Labeler code
- 11822
- Product ID
- 11822-3252_0fefb6bf-bc40-4f9e-a573-2dd50356fc38
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2021-09-24
- Marketing end
- 2026-12-30
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mucus Relief
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GUAIFENESIN | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 636522 |
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 |
|---|
| 11822-3252-7 | Mucus Relief | 40 in 1 CARTON | TABLET | 40 | | 3 |
| 11822-3252-7 | Mucus Relief | 1 in 1 BLISTER PACK | TABLET | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-3252 | MUCUS RELIEF (GUAIFENESIN) TABLET [RITE AID CORPORATION] | 2 | Current NDC, Legacy NDC, 2 package rows | 20230221_73fb2194-a582-4d3c-bc82-c5f110efcd81.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-3252-7 | 11822325207 | 40 BLISTER PACK in 1 CARTON (11822-3252-7) / 1 TABLET in 1 BLISTER PACK | 40 blister pack | 2021-09-24 | 2026-12-30 | No | No | Current |