Mucus Relief
- Product NDC
- 68391-724
- 11-digit product format
- 683910724
- Labeler code
- 68391
- Product ID
- 68391-724_3c120ab9-89a6-a9be-e063-6294a90a2b7c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- BJWC (Berkley & Jensen / BJ's)
- Application
- ANDA217780
- Marketing category
- ANDA
- Marketing start
- 2025-08-20
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mucus Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GUAIFENESIN | 1200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 310621 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68391-724-95 | Mucus Relief | 84 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 84 | | 2 |
| 68391-724-95 | Mucus Relief | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68391-724-95 | 68391072495 | 1 BOTTLE in 1 CARTON (68391-724-95) / 84 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2025-08-20 | No | No | Historical |