adult tussin chest congestion
- Product NDC
- 0363-1310
- 11-digit product format
- 003631310
- Labeler code
- 0363
- Product ID
- 0363-1310_e0f253e4-5392-4c5d-bc75-b4f61b9739f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-06-07
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-1310-34 | 00363131034 | 1 BOTTLE in 1 CARTON (0363-1310-34) > 237 mL in 1 BOTTLE | 1 bottle | 2022-06-07 | 0000-00-00 | No | No | Current |