Daytime Sinus Nighttime Sinus
- Product NDC
- 11673-694
- 11-digit product format
- 116730694
- Labeler code
- 11673
- Product ID
- 11673-694_6e30aed2-6c67-42d7-88c0-634d94cb6860
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, diphenhydramine HCl, guaifenesin, phenylephrine HCl
- Dosage form
- KIT
- Labeler
- Target Corporation
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-07-01
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-694 | DAYTIME SINUS NIGHTTIME SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, DIPHENHYDRAMINE HCL, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [TARGET CORPORATION] | 9 | Legacy NDC | 20240712_a2b9a91f-fb92-4b4a-8ec4-7002bba06be6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-694-09 | 11673069409 | 1 KIT in 1 CARTON (11673-694-09) * 8 TABLET, FILM COATED in 1 BLISTER PACK * 12 TABLET, FILM COATED in 1 BLISTER PACK | 1 kit | 2017-07-01 | 0000-00-00 | No | No | Current |