Roll On Anti-Perspirant Deodorant
- Product NDC
- 51870-001
- 11-digit product format
- 518700001
- Labeler code
- 51870
- Product ID
- 51870-001_47e5f195-d2d1-cacd-e063-6394a90a2adf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALUMINUM CHLOROHYDRATE
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Keefe Group
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-06-26
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 14 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
- Roll On Anti-Perspirant Deodorant
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLOROHYDRATE | 14 g/100mL |
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 |
|---|
| 51870-001-03 | Roll On Anti-Perspirant Deodorant | 88 mL in 1 BOTTLE, WITH APPLICATOR | SOLUTION | 88 | | 14 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51870-001 | ROLL ON ANTI-PERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) SOLUTION [KEEFE GROUP] | 13 | Current NDC, Legacy NDC, 1 package rows | 20241116_9a1bd5aa-8720-42fe-a157-d06d122a893c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51870-001-03 | 51870000103 | 88 mL in 1 BOTTLE, WITH APPLICATOR (51870-001-03) | 88 ml | 2012-06-26 | 0000-00-00 | No | No | Current |