DayTime Severe Congestion Relief and Nighttime Severe Cough and Congestion Relief
- Product NDC
- 69842-939
- 11-digit product format
- 698420939
- Labeler code
- 69842
- Product ID
- 69842-939_5e5f5af7-b360-4d6f-bad6-f92bb7edf99a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Daytime Acetaminophen, Guaifenesin, Phenylephrine HCI, NightTime Acetaminophen, Diphenhydramine HCI, Phenylephrine HCI
- Dosage form
- KIT
- Labeler
- CVS Pharmacy
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-04-30
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 69842-939-12 | 69842093912 | 1 KIT in 1 CARTON (69842-939-12) * 177 mL in 1 BOTTLE, PLASTIC * 177 mL in 1 BOTTLE, PLASTIC | 1 kit | 2018-04-30 | 0000-00-00 | No | No | Current |