Home NDC 10565-066 Roll On Anti Perspirant
Product NDC 10565-066
11-digit product format 105650066
Labeler code 10565
Product ID 10565-066_48334c7e-371c-00ff-e063-6394a90a3f42
Type HUMAN OTC DRUG
Nonproprietary name ALUMINUM CHLOROHYDRATE
Dosage form SOLUTION
Route TOPICAL
Labeler Hydrox Laboratories
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-10-26
Substance ALUMINUM CHLOROHYDRATE
Active strength 10 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Additional Listing Data#
Finished product Yes
Brand name base Roll On Anti Perspirant
Brand name suffix Alcohol Free
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 10565-066-01 Roll On Anti PerspirantAlcohol Free 45 mL in 1 BOTTLE, WITH APPLICATOR SOLUTION 45 12 10565-066-02 Roll On Anti PerspirantAlcohol Free 45 mL in 1 BOTTLE, WITH APPLICATOR SOLUTION 45 12
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10565-066 ROLL ON ANTI PERSPIRANT ALCOHOL FREE (ALUMINUM CHLOROHYDRATE) SOLUTION [HYDROX LABORATORIES] 11 Current NDC, Legacy NDC, 2 package rows 20231027_c5fb6769-23a3-4738-afe7-5ebbca4d9e69.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 1 of 74 · 1,465 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 10565-066-01 10565006601 45 mL in 1 BOTTLE, WITH APPLICATOR 45 ml Historical 10565-066-02 10565006602 45 mL in 1 BOTTLE, WITH APPLICATOR (10565-066-02) 45 ml 2011-10-26 0000-00-00 No No Current