Roll On Anti-Perspirant (Alcohol Free)

Manufacturer: Cardinal Health
Effective date: 2026-01-12
Label type: HUMAN OTC DRUG LABEL
Version: 13
Source: full-release
Hydrated at: 2026-06-01 01:32:16

Label at a glance#

ProductRoll On Anti-Perspirant (Alcohol Free)

Active ingredientALUMINUM CHLOROHYDRATE

Label structure8 sections

Dosage and administration

Apply to underarms only.

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

OTC - ASK DOCTOR SECTION

Ask a doctor before useif you have kidney disease.

OTC - STOP USE SECTION

Stop useif rash or irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children.If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 63517-803-45

deodorant +
antiperspirant

roll-on • scented

CardinalHealth

1.5 fl oz (45ml)

Principal Display Panel - 45ml Bottle Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63517-803-45	Roll On Anti-Perspirant (Alcohol Free)	45 mL in 1 BOTTLE, WITH APPLICATOR	SOLUTION	45		13

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 AT 1%)	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 (2000 MPA.S AT 1%)
GLYCERIN
POLYSORBATE 20
EDETATE SODIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63517-803	63517-803-45

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 (2000 MPA.S AT 1%)	S38J6RZN16	IACT
GLYCERIN	PDC6A3C0OX	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
EDETATE SODIUM	MP1J8420LU	IACT
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB

Source Document#

Source XML

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 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Edetate Sodium	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
Glycerin	GLYCERIN	PDC6A3C0OX	SOLUTION / TOPICAL		1971 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
Hydroxyethyl Cellulose (2000 MPA.S AT 1%)	HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)	S38J6RZN16	SOLUTION / TOPICAL	0.21 %w/v		Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
Glycerin	GLYCERIN	PDC6A3C0OX	SOLUTION / TOPICAL		1971 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
Hydroxyethyl Cellulose (2000 MPA.S AT 1%)	HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)	S38J6RZN16	SOLUTION / TOPICAL	0.21 %w/v		Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
Polysorbate 20	POLYSORBATE 20	7T1F30V5YH	SOLUTION / TOPICAL	15 %w/w		Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
Polysorbate 20	POLYSORBATE 20	7T1F30V5YH	SOLUTION / TOPICAL	15 %w/w		Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
Edetate Sodium	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii+route+dosage form 2 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	Cardinal Health	00281593-ae46-4936-ba86-129ee9d75e40	2026-01-12	Warnings	Exact identifier ndc (package): 63517-803-45 ndc (product): 63517-803 ndc11 (package): 63517080345 spl id: 4833ac62-bb24-887c-e063-6294a90aca4a spl set id: 00281593-ae46-4936-ba86-129ee9d75e40

Reported adverse events (FAERS/openFDA)#

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