MDS Roll-On Anti-Perspirant
- Product NDC
- 87119-001
- 11-digit product format
- 871190001
- Labeler code
- 87119
- Product ID
- 87119-001_4340f1c6-a2eb-b885-e063-6394a90a0cae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chlorohydrate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- MDS GLOBAL FZE
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-23
- Substance
- ALUMINUM CHLOROHYDRATE ANHYDROUS
- Active strength
- 15.4 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MDS Roll-On Anti-Perspirant
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLOROHYDRATE ANHYDROUS | 15.4 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 407PSC3OC7 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87119-001-01 | MDS Roll-On Anti-Perspirant | 50 mL in 1 BOTTLE | CREAM | 50 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87119-001-01 | 87119000101 | 50 mL in 1 BOTTLE (87119-001-01) | 50 ml | 2025-09-23 | No | No | Historical |