Hi and Dri Roll On
- Product NDC
- 10967-786
- 11-digit product format
- 109670786
- Labeler code
- 10967
- Product ID
- 10967-786_2a99b834-0c9b-6f97-e063-6394a90a8407
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chlorohydrate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Revlon Consumer Products Corp
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-01-01
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- .18 g/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hi and Dri Roll On
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLOROHYDRATE | .18 g/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 |
|---|
| 10967-786-17 | Hi and Dri Roll On | 50 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10967-786 | HI AND DRI ROLL ON (ALUMINUM CHLOROHYDRATE) LIQUID [REVLON CONSUMER PRODUCTS CORP] | 1 | Current NDC, 1 package rows | 20250101_2a998081-6433-8228-e063-6294a90adc3d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 10967-786-17 | 10967078617 | 50 mL in 1 BOTTLE, WITH APPLICATOR (10967-786-17) | 50 ml | 2022-01-01 | No | No | Current |