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- Product NDC
- 11673-477
- 11-digit product format
- 116730477
- Labeler code
- 11673
- Product ID
- 11673-477_aeebfcb8-e3e0-4894-9355-4ecd06915906
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine Hydrochloride, Guaifenesin
- Dosage form
- KIT
- Labeler
- Target Corporation
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-08-15
- 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 |
|---|
| 11673-477-02 | 11673047702 | 1 KIT in 1 PACKAGE (11673-477-02) * 355 mL in 1 BOTTLE (11673-251-40) * 355 mL in 1 BOTTLE | 1 kit | 2019-08-15 | 0000-00-00 | No | No | Current |