Dr Sweat

Product NDC
64942-1633
11-digit product format
649421633
Labeler code
64942
Product ID
64942-1633_ef3f84ad-9d66-b242-e053-2a95a90ac876
Type
HUMAN OTC DRUG
Nonproprietary name
Aluminum Chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Conopco Inc. d/b/a/ Unilever
Application
part350
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2019-03-29
Marketing end
0000-00-00
Substance
ALUMINUM CHLORIDE
Active strength
15 g/100g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1633-12025-01-30C16284748780-12cef2736-8b9b-d83d-e063-dadaa90ab31fDr Sweat Clinical Strength Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1633-1Dr Sweat0.0284 g in 1 PACKETLIQUID0.02842

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1633DR SWEAT (ALUMINUM CHLORIDE) LIQUID [CONOPCO INC. D/B/A/ UNILEVER]2Legacy NDC, 1 package rows20221208_822ef329-f042-54c4-e053-2991aa0ac753.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
64942-1633-164942163301.0284 g in 1 PACKET (64942-1633-1) 2019-03-290000-00-00NoNoCurrent