Dove
- Product NDC
- 64942-1578
- 11-digit product format
- 649421578
- Labeler code
- 64942
- Product ID
- 64942-1578_253bd708-f288-aecc-e063-6294a90a382d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Powder Roll-On AntiPerspirant Deodorant
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Conopco Inc. d/b/a/ Unilever
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-10-30
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 22 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
- Dove
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLOROHYDRATE | 22 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | HPN8MZW13M |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 64942-1578-1 | Dove | 74 mL in 1 CONTAINER | LIQUID | 74 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64942-1578 | DOVE (POWDER ROLL-ON ANTIPERSPIRANT DEODORANT) LIQUID [CONOPCO INC. D/B/A/ UNILEVER] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241027_69749de7-cae0-f339-e053-2a91aa0a3339.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64942-1578-1 | 64942157801 | 74 mL in 1 CONTAINER (64942-1578-1) | 74 ml | 2020-10-30 | 0000-00-00 | No | No | Current |