Vicks Sinex D
- Product NDC
- 37000-921
- 11-digit product format
- 370000921
- Labeler code
- 37000
- Product ID
- 37000-921_a60103b7-a911-8a3d-e053-2a95a90a8831
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Phenylephrine Hydrochloride, Doxylamine Succinate, and Dextromethorphan Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- ANDA076518
- Marketing category
- ANDA
- Marketing start
- 2018-12-17
- Marketing end
- 2021-03-01
- Substance
- PSEUDOEPHEDRINE HYDROCHLORIDE; NAPROXEN SODIUM
- Active strength
- 120 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 37000-921 | VICKS SINEX D SEVERE SINUS AND COLD (ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE, AND DEXTROMETHORPHAN HYDROBROMIDE) TABLET [THE PROCTER & GAMBLE MANUFACTURING COMPANY] | 2 | Legacy NDC | 20200520_7d3ee6a9-e482-af6a-e053-2a91aa0a64d6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37000-921-30 | 37000092130 | 3 BLISTER PACK in 1 CARTON (37000-921-30) > 10 TABLET in 1 BLISTER PACK | 3 blister pack | 2018-12-17 | 2021-03-01 | No | No | Current |