Tussin Multi Symptom Cold CF
- Product NDC
- 68788-6872
- 11-digit product format
- 687886872
- Labeler code
- 68788
- Product ID
- 68788-6872_1bc52f51-cc25-41f4-b227-1bcde7d6dede
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin, Phenylephrine
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-01-19
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 20 mg/10mL; mg/10mL; mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6872-1 | 68788687201 | 1 BOTTLE, PLASTIC in 1 BOX (68788-6872-1) > 118 mL in 1 BOTTLE, PLASTIC | 2017-01-19 | 0000-00-00 | No | No | Current |