DawnMist Antiperspirant Deodorant
- Product NDC
- 65517-1021
- 11-digit product format
- 655171021
- Labeler code
- 65517
- Product ID
- 65517-1021_1dec6ed8-c5c3-856e-e063-6394a90a8850
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALUMINUM CHLOROHYDRATE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Dukal LLC
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-10-12
- Marketing end
- 2027-03-25
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 78 mg/mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DawnMist Antiperspirant Deodorant
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLOROHYDRATE | 78 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | HPN8MZW13M |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65517-1021-1 | DawnMist Antiperspirant Deodorant | 44 mL in 1 BOTTLE, WITH APPLICATOR | LOTION | 44 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65517-1021 | DAWNMIST ANTIPERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) LOTION [DUKAL LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240724_3ea33bd5-f977-4bff-9614-52e081a6ed3f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65517-1021-1 | 65517102101 | 44 mL in 1 BOTTLE, WITH APPLICATOR (65517-1021-1) | 44 ml | 2018-10-12 | 2027-03-25 | No | No | Current |