Mucus Relief
- Product NDC
- 69256-731
- 11-digit product format
- 692560731
- Labeler code
- 69256
- Product ID
- 69256-731_f699deee-83c7-4332-a56e-91a6d3331fc9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Harris Teeter, LLC
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2023-02-06
- Marketing end
- 2026-10-28
- 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69256-731-20 | Mucus Relief | 1 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 1 | | 3 |
| 69256-731-20 | Mucus Relief | 20 in 1 CARTON | TABLET, EXTENDED RELEASE | 20 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69256-731 | MUCUS RELIEF (GUAIFENESIN) TABLET, EXTENDED RELEASE [HARRIS TEETER, LLC] | 1 | Current NDC, 2 package rows | 20240806_f7f2e64c-0fb9-413d-80ed-4d7cc2a07e0c.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 |
|---|
| 69256-731-20 | 69256073120 | 20 BLISTER PACK in 1 CARTON (69256-731-20) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 20 blister pack | 2023-02-06 | 2026-10-28 | No | No | Historical |