Home NDC 10565-074 Anti-Perspirant Deodorant Roll-On
Product NDC 10565-074
11-digit product format 105650074
Labeler code 10565
Product ID 10565-074_48335166-d88f-5394-e063-6394a90a03b4
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chlorohydrate
Dosage form LIQUID
Route TOPICAL
Labeler Hydrox Laboratories
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-03-20
Substance ALUMINUM CHLOROHYDRATE
Active strength 10 g/100mL
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 Roll-On
Brand name suffix Unscented
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE 10 g/100mL
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 10565-074-01 Anti-Perspirant Deodorant Roll-OnUnscented 45 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 45 12 10565-074-02 Anti-Perspirant Deodorant Roll-OnUnscented 59 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 59 12
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10565-074 ANTI-PERSPIRANT DEODORANT ROLL-ON UNSCENTED (ALUMINUM CHLOROHYDRATE) LIQUID [HYDROX LABORATORIES] 11 Current NDC, Legacy NDC, 2 package rows 20231027_a3454d37-ded4-40db-a6b4-c56255796fca.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 10565-074-01 10565007401 45 mL in 1 BOTTLE, WITH APPLICATOR (10565-074-01) 45 ml 2012-03-20 0000-00-00 No No Current 10565-074-02 10565007402 59 mL in 1 BOTTLE, WITH APPLICATOR (10565-074-02) 59 ml 2012-03-20 0000-00-00 No No Current