DawnMist Antiperspirant Deodorant
- Product NDC
- 65517-1014
- 11-digit product format
- 655171014
- Labeler code
- 65517
- Product ID
- 65517-1014_735710be-5ba5-6452-e053-2991aa0a9686
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALUMINUM CHLOROHYDRATE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Dukal Corporation
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-05-02
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 45 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65517-1014 | DAWNMIST ANTIPERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) GEL [DUKAL LLC] | 4 | Legacy NDC | 20240724_791fa688-d0ea-42a1-b4ba-e79559431cae.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65517-1014-1 | 65517101401 | 3 mL in 1 PACKET (65517-1014-1) | 3 ml | 2017-09-08 | 0000-00-00 | No | No | Current |