Daytime Sinus Relief and Nighttime Sinus Relief
- Product NDC
- 51013-114
- 11-digit product format
- 510130114
- Labeler code
- 51013
- Product ID
- 51013-114_d5317ab7-9040-4a2a-bd6e-570abd6afc9e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, doxylamine succinate, phenylephrine hydrochloride
- Dosage form
- KIT
- Labeler
- PuraCap Pharmaceutical LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-08-02
- Marketing end
- 2019-12-31
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record