Axe
- Product NDC
- 64942-1518
- 11-digit product format
- 649421518
- Labeler code
- 64942
- Product ID
- 64942-1518_b0920fd8-5405-c7a6-e053-2a95a90a28ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Forest Dry Spray Antiperspirant
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Conopco Inc. d/b/a/ Unilever
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-09-11
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 23 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 64942-1518-1 | Axe | 107 g in 1 CAN | AEROSOL, SPRAY | 107 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64942-1518 | AXE (FOREST DRY SPRAY ANTIPERSPIRANT) AEROSOL, SPRAY [CONOPCO INC. D/B/A/ UNILEVER] | 3 | Legacy NDC, 1 package rows | 20201001_58fd5571-37d8-7f10-e053-2991aa0afdce.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64942-1518-1 | 64942151801 | 107 g in 1 CAN (64942-1518-1) | 107 g | 2017-09-11 | 0000-00-00 | No | No | Current |