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- Product NDC
- 11673-619
- 11-digit product format
- 116730619
- Labeler code
- 11673
- Product ID
- 11673-619_cc038336-7d0f-4f4f-ba49-cb169506550e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, diphenhydramine, guaifenesin, phenylephrine HCl
- Dosage form
- KIT
- Labeler
- Target Corporation
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-06-30
- Marketing end
- 2019-10-31
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record