DawnMist Antiperspirant Deodorant
- Product NDC
- 65517-1010
- 11-digit product format
- 655171010
- Labeler code
- 65517
- Product ID
- 65517-1010_7bbc44e2-c9f7-408a-e053-2a91aa0ab037
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALUMINUM CHLOROHYDRATE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Dukal Corporation
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-01-10
- Marketing end
- 2021-09-28
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 45 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 65517-1010-1 | 65517101001 | 44 mL in 1 BOTTLE, WITH APPLICATOR (65517-1010-1) | 44 ml | 2013-01-10 | 2021-09-28 | No | No | Current |