DawnMist Antiperspirant
- Product NDC
- 65517-2031
- 11-digit product format
- 655172031
- Labeler code
- 65517
- Product ID
- 65517-2031_29a89490-b70d-4a41-e063-6294a90a90ea
- 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
- 2024-08-30
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 45 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DawnMist Antiperspirant
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLOROHYDRATE | 45 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 |
|---|
| 65517-2031-1 | DawnMist Antiperspirant | 44 mL in 1 BOTTLE | LOTION | 44 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65517-2031 | DAWNMIST ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) LOTION [DUKAL LLC] | 2 | Current NDC, 1 package rows | 20241222_1e17daf8-075e-e331-e063-6294a90ad11c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 65517-2031-1 | 65517203101 | 44 mL in 1 BOTTLE (65517-2031-1) | 44 ml | 2024-08-30 | No | No | Current |