Adult Tussin
- Product NDC
- 69230-332
- 11-digit product format
- 692300332
- Labeler code
- 69230
- Product ID
- 69230-332_62155505-522d-4269-8d03-599c6d2c902c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GUAIFENESIN
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Camber Consumer Care
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-05-19
- Substance
- GUAIFENESIN
- Active strength
- 200 mg/10mL
- 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
- Adult Tussin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GUAIFENESIN | 200 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 310604 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69230-332-23 | Adult Tussin | 237 mL in 1 BOTTLE | SOLUTION | 237 | | 1 |
| 69230-332-23 | Adult Tussin | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69230-332 | ADULT TUSSIN (GUAIFENESIN) SOLUTION [CAMBER CONSUMER CARE] | 1 | Current NDC, 2 package rows | 20250523_896d2540-279a-4405-b176-acbff56303e5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69230-332-23 | 69230033223 | 1 BOTTLE in 1 CARTON (69230-332-23) / 237 mL in 1 BOTTLE | 1 bottle | 2025-05-20 | No | No | Current |