DawnMist Antiperspirant Deodorant
- Product NDC
- 65517-1005
- Requested package NDC
- 65517-1005-1
- 11-digit product format
- 655171005
- Labeler code
- 65517
- Product ID
- 65517-1005_77e5b86d-9f02-8bec-e053-2991aa0a352a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALUMINUM CHLOROHYDRATE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Dukal Corporation
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-01-10
- 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
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65517-1005-1 | DawnMist Antiperspirant Deodorant | 59 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 59 | | 10 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65517-1005 | DAWNMIST ANTIPERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) LIQUID [DUKAL LLC] | 10 | Legacy NDC, 1 package rows | 20240724_5599d92f-c2d8-4398-baaa-6c86d76bebde.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65517-1005-1 | 65517100501 | 59 mL in 1 BOTTLE, WITH APPLICATOR (65517-1005-1) | 59 ml | 2013-01-10 | 0000-00-00 | No | No | Current |