ZONSEN Antiperspirant
- Product NDC
- 72932-010
- 11-digit product format
- 729320010
- Labeler code
- 72932
- Product ID
- 72932-010_1fb8e1a7-5478-a040-e063-6294a90a2643
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chlorohydrate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Wuhan Zonsen Medical Products Co., Ltd.
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-08-15
- 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
- ZONSEN 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 |
|---|
| 72932-010-01 | ZONSEN Antiperspirant | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72932-010 | ZONSEN ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) LIQUID [WUHAN ZONSEN MEDICAL PRODUCTS CO., LTD.] | 1 | Current NDC, 1 package rows | 20240824_1fb8e1a7-5477-a040-e063-6294a90a2643.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72932-010-01 | 72932001001 | 59 mL in 1 BOTTLE, PLASTIC (72932-010-01) | 59 ml | 2024-08-15 | No | No | Current |