Roll-On Antiperspirant Deodorant - Scented

Manufacturer: O&M HALYARD, INC.
Effective date: 2025-10-09
Label type: HUMAN OTC DRUG LABEL
Version: 17
Source: full-release
Hydrated at: 2026-06-01 01:38:27

Label at a glance#

ProductRoll-On Antiperspirant Deodorant - Scented

Active ingredientALUMINUM CHLOROHYDRATE

Label structure9 sections

Dosage and administration

Apply to underarms only. 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. For external use only.

OTC - DO NOT USE SECTION

Do not use on broken skin. Stop use if rash or irritation occurs. kidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed. Ask a doctor before use if you have

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only. Use daily for best results.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Hydroxyethyl Cellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA

SPL UNCLASSIFIED SECTION

Distributed by Owens & Minor 9120 Lockwood Blvd. Mechanicsville, VA 23116

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MEDICHOICE^®

ROLL-ON ANTIPERSPIRANT DEODORANT

CLEAN FRESH SCENT

FIGHTS WETNESS

1.5 fl. oz. (45 mL.)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
39892-0807-0	Roll-On Antiperspirant Deodorant - Scented	45 mL in 1 BOTTLE, WITH APPLICATOR	SOLUTION	45		17

Products#

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

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

Roll-On Antiperspirant Deodorant - Scented
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
39892-0807	39892-0807-0

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

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
16	2024-11-14	full-release	2026-06-01 00:37:17

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 Antiperspirant Deodorant - Scented	ALUMINUM CHLOROHYDRATE	O&M HALYARD, INC.	18191440-1fd4-4d1a-8cf0-a79f9853bbcc	2025-10-09	Warnings	Exact identifier ndc (package): 39892-0807-0 ndc (product): 39892-0807 ndc11 (package): 39892080700 spl id: 40b3966f-d6ee-d298-e063-6394a90a509d spl set id: 18191440-1fd4-4d1a-8cf0-a79f9853bbcc

Reported adverse events (FAERS/openFDA)#

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