Adult Tussin Expectorant
- Product NDC
- 63868-039
- 11-digit product format
- 638680039
- Labeler code
- 63868
- Product ID
- 63868-039_dee265b9-c87e-465a-8112-5cf4b1c381b3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GUAIFENESIN
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Chain Drug Marketing Association, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-09-07
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 100 mg/5mL
- 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 |
|---|
| 63868-039-04 | 63868003904 | 1 BOTTLE in 1 CARTON (63868-039-04) > 118 mL in 1 BOTTLE | 1 bottle | 2022-06-27 | 0000-00-00 | No | No | Current |