Roll On Anti Perspirant

Manufacturer: Hydrox Laboratories
Effective date: 2026-01-12
Label type: HUMAN OTC DRUG LABEL
Version: 12
Source: full-release
Hydrated at: 2026-06-01 01:32:21

Label at a glance#

ProductRoll On Anti Perspirant Alcohol Free

Active ingredientALUMINUM CHLOROHYDRATE

Label structure8 sections

Dosage and administration

Apply to underarms. Use daily for best results.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate, 10% - Anhydrous Basis

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness.

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

OTC - DO NOT USE SECTION

Do not use on broken skin.

OTC - STOP USE SECTION

Stop use if rash or irritation occurs.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you havekidney disease.

OTC - WHEN USING SECTION

If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms. Use daily for best results.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Personal Care

Fresh Moment

Anti-Perspirant
Deodorant Roll-On
Alcohol-Free

Helps Reduce Wetness
Spring Fresh Fragrance

MADE IN USA

1.5 FL. OZ. (45mL)

Principal Display Panel - 45 mL Bottle Label

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0021599412517	GTIN-13: 0021599412517 EAN-13: 0021599412517 GTIN-12: 021599412517 UPC-A: 021599412517 GTIN storage (14 digits): 00021599412517	roll-on-01.jpg

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	SPL version
ALUMINUM CHLOROHYDRATE	ACTIVE INGREDIENT	HPN8MZW13M	1
ALUMINUM CHLOROHYDRATE	ACTIVE MOIETY	HPN8MZW13M	1
Edetate Sodium	INACTIVE INGREDIENT	MP1J8420LU	1
Glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	1
Hydroxyethyl Cellulose (2000 MPA.S FOR 1% Aqueous Solution)	INACTIVE INGREDIENT	S38J6RZN16	1
Polysorbate 20	INACTIVE INGREDIENT	7T1F30V5YH	1
Water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Roll On Anti Perspirant Alcohol Free
ALUMINUM CHLOROHYDRATE
WATER
HYDROXYETHYL CELLULOSE, UNSPECIFIED
GLYCERIN
POLYSORBATE 20
EDETATE SODIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10565-066	10565-066-02, 10565-066-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
HYDROXYETHYL CELLULOSE, UNSPECIFIED	T4V6TWG28D	IACT
GLYCERIN	PDC6A3C0OX	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
EDETATE SODIUM	MP1J8420LU	IACT
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Polysorbate 20	POLYSORBATE 20	7T1F30V5YH	SOLUTION / TOPICAL	15 %w/w		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Glycerin	GLYCERIN	PDC6A3C0OX	SOLUTION / TOPICAL		1971 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Edetate Sodium	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Edetate Sodium	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Polysorbate 20	POLYSORBATE 20	7T1F30V5YH	SOLUTION / TOPICAL	15 %w/w		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Hydroxyethyl Cellulose (2000 MPA.S FOR 1% Aqueous Solution)	HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)	S38J6RZN16	SOLUTION / TOPICAL	0.21 %w/v		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Polysorbate 20	POLYSORBATE 20	7T1F30V5YH	SOLUTION / TOPICAL	15 %w/w		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Hydroxyethyl Cellulose (2000 MPA.S FOR 1% Aqueous Solution)	HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)	S38J6RZN16	SOLUTION / TOPICAL	0.21 %w/v		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Glycerin	GLYCERIN	PDC6A3C0OX	SOLUTION / TOPICAL		1971 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Hydroxyethyl Cellulose (2000 MPA.S FOR 1% Aqueous Solution)	HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)	S38J6RZN16	SOLUTION / TOPICAL	0.21 %w/v		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Edetate Sodium	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
Glycerin	GLYCERIN	PDC6A3C0OX	SOLUTION / TOPICAL		1971 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates

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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Roll On Anti Perspirant Alcohol Free	ALUMINUM CHLOROHYDRATE	Hydrox Laboratories	c5fb6769-23a3-4738-afe7-5ebbca4d9e69	2026-01-12	Warnings	Exact identifier ndc (package): 10565-066-02 ndc (package): 10565-066-01 ndc (product): 10565-066 ndc11 (package): 10565006602 ndc11 (package): 10565006601 spl id: 48334c7e-371c-00ff-e063-6394a90a3f42 spl set id: c5fb6769-23a3-4738-afe7-5ebbca4d9e69

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.