Home NDC 68599-2304 Anti-Perspirant Deodorant
Product NDC 68599-2304
11-digit product format 685992304
Labeler code 68599
Product ID 68599-2304_48355fe4-49c0-3ad4-e063-6294a90a215f
Type HUMAN OTC DRUG
Nonproprietary name ALUMINUM CHLOROHYDRATE
Dosage form SPRAY
Route TOPICAL
Labeler McKesson Medical-Surgical Inc.
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-10-09
Substance ALUMINUM CHLOROHYDRATE
Active strength 130 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Anti-Perspirant Deodorant
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE 130 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination HPN8MZW13M Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68599-2304-1 Anti-Perspirant Deodorant 59 mL in 1 BOTTLE, SPRAY SPRAY 59 14 68599-2304-2 Anti-Perspirant Deodorant 118 mL in 1 BOTTLE, SPRAY SPRAY 118 14
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68599-2304 ANTI-PERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) SPRAY [MCKESSON MEDICAL-SURGICAL INC.] 12 Current NDC, Legacy NDC, 2 package rows 20241116_aae7f100-713b-4b4e-92cf-cab68f740e14.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 70 of 73 · 1,450 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68599-2304-1 68599230401 59 mL in 1 BOTTLE, SPRAY (68599-2304-1) 59 ml 2017-10-19 0000-00-00 No No Current 68599-2304-2 68599230402 118 mL in 1 BOTTLE, SPRAY (68599-2304-2) 118 ml 2017-10-19 0000-00-00 No No Current