Hand Antiperspirant Nightly Use
- Product NDC
- 74307-008
- 11-digit product format
- 743070008
- Labeler code
- 74307
- Product ID
- 74307-008_4bbe7193-beab-33e8-e063-6394a90a5bff
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chloride Hexahydrate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Clutch Inc
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-06-01
- Substance
- ALUMINUM CHLORIDE
- Active strength
- 15 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hand Antiperspirant Nightly Use
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLORIDE | 15 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3CYT62D3GA |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 74307-008-01 | Hand Antiperspirant Nightly Use | 30 mL in 1 BOTTLE, PUMP | CREAM | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 74307-008 | HAND ANTIPERSPIRANT NIGHTLY USE (ALUMINUM CHLORIDE HEXAHYDRATE) CREAM [CLUTCH INC] | 1 | Current NDC, Legacy NDC, 1 package rows | 20200604_a70d9eff-b5a3-5c52-e053-2a95a90a704c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 74307-008-01 | 74307000801 | 30 mL in 1 BOTTLE, PUMP (74307-008-01) | 30 ml | 2020-06-01 | 0000-00-00 | No | No | Current |