Axe

Product NDC
64942-1514
11-digit product format
649421514
Labeler code
64942
Product ID
64942-1514_b0908876-277c-7ba8-e053-2a95a90af248
Type
HUMAN OTC DRUG
Nonproprietary name
Axe Charge Up 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 NDCProductDescriptionFormQuantityStrengthSPL version
64942-1514-1Axe107 g in 1 CANAEROSOL, SPRAY1072

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1514AXE (AXE CHARGE UP DRY SPRAY ANTIPERSPIRANT) AEROSOL, SPRAY [CONOPCO INC. D/B/A/ UNILEVER]2Legacy NDC, 1 package rows20201001_58fd5571-37c8-7f10-e053-2991aa0afdce.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
64942-1514-164942151401107 g in 1 CAN (64942-1514-1) 107 g2017-09-110000-00-00NoNoCurrent