Day and Night Cold
- Product NDC
- 57344-147
- 11-digit product format
- 573440147
- Labeler code
- 57344
- Product ID
- 57344-147_d10f835d-c53b-4083-960a-fdaddb965db0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride
- Dosage form
- KIT
- Labeler
- AAA Pharmaceutical, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-12-28
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record