Non Drowsy DAY Cold and Flu Plus and NIGHTTIME Cold and Flu Plus
- Product NDC
- 68210-1111
- 11-digit product format
- 682101111
- Labeler code
- 68210
- Product ID
- 68210-1111_ee15b8fa-6eb2-ec11-e053-2995a90a0660
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride
- Dosage form
- KIT
- Labeler
- Spirit Pharmaceuticals LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-03-11
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68210-1111-2 | 68210111102 | 1 KIT in 1 CARTON (68210-1111-2) * 1 BLISTER PACK in 1 CARTON > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 kit | 2020-03-11 | 0000-00-00 | No | No | Current |