VENROCK
- Product NDC
- 85772-0003
- 11-digit product format
- 857720003
- Labeler code
- 85772
- Product ID
- 85772-0003_3862d1b8-d4b2-480c-e063-6394a90a78ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chlorohydrate Spray
- Dosage form
- SPRAY
- Route
- CUTANEOUS; TOPICAL
- Labeler
- Guangzhou Oupeng Cosmetics Co., Ltd.
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-27
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 10 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- VENROCK
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLOROHYDRATE | 10 g/100g |
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 |
|---|
| 85772-0003-1 | VENROCK | 1 g in 1 CARTON | SPRAY | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85772-0003-1 | 85772000301 | 1 g in 1 CARTON (85772-0003-1) | 1 g | 2025-06-27 | No | No | Historical |