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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	10565-066	10565-066-01	D	Discontinued by firm		2026-10-23

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…`

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: 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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
c5fb6769-23a3-4738-afe7-5ebbca4d9e69	Available on FDA.report

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#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ALUMINUM CHLOROHYDRATE	ACTIVE INGREDIENT	HPN8MZW13M	ROLL ON ANTI PERSPIRANT (ALUMINUM CHLOROHYDRATE) SOLUTION [HYDROX LABORATORIES]	1
ALUMINUM CHLOROHYDRATE	ACTIVE MOIETY	HPN8MZW13M	ROLL ON ANTI PERSPIRANT (ALUMINUM CHLOROHYDRATE) SOLUTION [HYDROX LABORATORIES]	1
Edetate Sodium	INACTIVE INGREDIENT	MP1J8420LU	ROLL ON ANTI PERSPIRANT (ALUMINUM CHLOROHYDRATE) SOLUTION [HYDROX LABORATORIES]	1
Glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	ROLL ON ANTI PERSPIRANT (ALUMINUM CHLOROHYDRATE) SOLUTION [HYDROX LABORATORIES]	1
Hydroxyethyl Cellulose (2000 MPA.S FOR 1% Aqueous Solution)	INACTIVE INGREDIENT	S38J6RZN16	ROLL ON ANTI PERSPIRANT (ALUMINUM CHLOROHYDRATE) SOLUTION [HYDROX LABORATORIES]	1
Polysorbate 20	INACTIVE INGREDIENT	7T1F30V5YH	ROLL ON ANTI PERSPIRANT (ALUMINUM CHLOROHYDRATE) SOLUTION [HYDROX LABORATORIES]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	ROLL ON ANTI PERSPIRANT (ALUMINUM CHLOROHYDRATE) SOLUTION [HYDROX LABORATORIES]	1

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 73 of 73 · 1,450 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Vanicream Anti-perspirant/Deodorant	ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY	Pharmaceutical Specialties, Inc.	3da5c528-4b39-4e6a-e054-00144ff88e88	2023-10-02	Warnings	Exact identifier application number: M019
Lady Speed Stick Invisible Dry Shower Fresh Antiperspirant Deodorant	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	COLGATE PALMOLIVE COMPANY	c4d773bd-a339-431b-a5b4-21a2728bcfcf	2021-05-20	Warnings	Exact identifier application number: M019
Speed Stick Power Ultimate Sport	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	Colgate-Palmolive Company	773c0fe1-bdf6-49bd-bff1-c199dcd61b28	2021-05-20	Warnings	Exact identifier application number: M019
Speed Stick Unscented Antiperspirant Deodorant	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	Colgate-Palmolive Company	28d9705f-d0f9-4cc9-a691-268ea2a39bf0	2021-05-18	Warnings	Exact identifier application number: M019
Speed Stick Fresh Antiperspirant Deodorant	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	COLGATE PALMOLIVE COMPANY	9754c8a2-526b-4246-99ae-4b96f7822e66	2021-05-17	Warnings	Exact identifier application number: M019
Speed Stick Cool Clean	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	Colgate-Palmolive Company	137ce9d6-1ce4-46d3-92a9-34d0097d9e38	2021-05-17	Warnings	Exact identifier application number: M019
Lady Speed Stick Invisible Dry	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	COLGATE PALMOLIVE COMPANY	401c5590-0cfd-4bf5-8815-24f8df7adc74	2021-04-02	Warnings	Exact identifier application number: M019
Lady Speed Stick Teen Spirit Pink Crush	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	Colgate-Palmolive Company	46ffe45b-b637-4635-abbc-a0280a6a9bbe	2020-01-14	Warnings	Exact identifier application number: M019
Speed Stick Irish Spring Original	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	Colgate-Palmolive Company	dcd2f0b2-ac23-4e99-9244-22c3f616abf4	2019-12-27	Warnings	Exact identifier application number: M019
Lady Speed Stick Double Defense Floral Fresh - antiperspirant/deodorant	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	COLGATE PALMOLIVE COMPANY	fa89befd-b7fe-4019-80cf-ddbf8295c2c5	2019-12-16	Warnings	Exact identifier application number: M019

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
HPN8MZW13M	ALUMINUM CHLOROHYDRATE	12359-72-7	ALUMINUM CHLOROHYDRATE

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Anti-Perspirant Deodorant Roll-On Alcohol-Free	Hydrox Laboratories	2026-01-12	HUMAN OTC DRUG LABEL	12