DAYTIME and Nighttime Sinus Relief
- Product NDC
- 0363-2210
- 11-digit product format
- 003632210
- Labeler code
- 0363
- Product ID
- 0363-2210_a22a9719-79f5-2ef6-e053-2a95a90ad5d1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE,GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE / ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- KIT
- Labeler
- Walgreens
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-02-04
- Marketing end
- 0000-00-00
- Active strength
- 0
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-2210-24 | 00363221024 | 1 KIT in 1 PACKAGE, COMBINATION (0363-2210-24) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 kit | 2020-02-06 | 0000-00-00 | No | No | Current |