Ban

Manufacturer: Kao USA Inc
Effective date: 2023-03-28
Label type: HUMAN OTC DRUG LABEL
Version: 8
Source: legacy-cache
Hydrated at: 2026-08-01 21:33:43

Label at a glance#

ProductBan Roll-On Antiperspirant Deodorant Simple Clean

Active ingredientALUMINUM CHLOROHYDRATE

Label structure14 sections

Storage and handling

Other information store at room temperature

Contacts and useful links#

PhoneLabel contact1-866-226-3363

Websitewww.bandeodorant.com

www.bandeodorant.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum chlorohydrate 18%

OTC - PURPOSE SECTION

Purpose

Antiperspirant

INDICATIONS & USAGE SECTION

Use

reduces underarm perspiration

WARNINGS SECTION

Warnings

For external use only

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 have kidney disease

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 right away.

DOSAGE & ADMINISTRATION SECTION

Directions

apply to underarms only

STORAGE AND HANDLING SECTION

Other information

store at room temperature

INACTIVE INGREDIENT SECTION

Inactive ingredients

water, PPG-11 stearyl ether, steareth-2, steareth-20, fragrance, helianthus annuus (sunflower) seed oil, phellodendron amurense bark extract, hordeum distichon (barley) extract, santalum album (sandalwood) extract

SPL UNCLASSIFIED SECTION

Questions? 1-866-226-3363

www.bandeodorant.com

BAN is a trademark of Kao Corp.

Dist. by Kao USA Inc. Cincinnati, OH 45214

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ban

simply clean

INVISIBLE ROLL-ON

CRUELTY FREE • PARABEN FREE • DYE FREE

antiperspirant deodorant

3.5 FL OZ (103 mL)

10596-400-35 UPDATED

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALUMINUM CHLOROHYDRATE	ACTIVE INGREDIENT	HPN8MZW13M	1
ALUMINUM CHLOROHYDRATE	ACTIVE MOIETY	HPN8MZW13M	1
BARLEY	INACTIVE INGREDIENT	5PWM7YLI7R	1
PHELLODENDRON AMURENSE BARK	INACTIVE INGREDIENT	PBG27B754G	1
SANDALWOOD	INACTIVE INGREDIENT	3641YW25N2	1
STEARETH-2	INACTIVE INGREDIENT	V56DFE46J5	1
STEARETH-20	INACTIVE INGREDIENT	L0Q8IK9E08	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Ban Roll-On Antiperspirant Deodorant Simple Clean
Aluminum Chlorohydrate
PPG-11 STEARYL ETHER
WATER
STEARETH-2
STEARETH-20
SANDALWOOD
PHELLODENDRON AMURENSE BARK
BARLEY
SUNFLOWER OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10596-400	10596-400-35, 10596-400-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PPG-11 STEARYL ETHER	S4G2J0Y0LG	IACT
WATER	059QF0KO0R	IACT
STEARETH-2	V56DFE46J5	IACT
STEARETH-20	L0Q8IK9E08	IACT
SANDALWOOD	3641YW25N2	IACT
PHELLODENDRON AMURENSE BARK	PBG27B754G	IACT
BARLEY	5PWM7YLI7R	IACT
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB
SUNFLOWER OIL	3W1JG795YI	IACT

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 · 5 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
STEARETH-2	STEARETH-2	V56DFE46J5	AEROSOL, FOAM / TOPICAL	1.09 %w/w		Exact identifier — unii candidate 4 equally ranked IID candidates
STEARETH-2	STEARETH-2	V56DFE46J5	LOTION / TOPICAL	0.4 %w/w		Exact identifier — unii candidate 4 equally ranked IID candidates
STEARETH-20	STEARETH-20	L0Q8IK9E08	CREAM / TOPICAL	4.15 %w/w		Exact identifier — unii candidate
STEARETH-2	STEARETH-2	V56DFE46J5	OINTMENT / TOPICAL		714 mg	Exact identifier — unii candidate 4 equally ranked IID candidates
STEARETH-2	STEARETH-2	V56DFE46J5	CREAM / TOPICAL		643 mg	Exact identifier — unii candidate 4 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
2b205287-dfd3-75fe-e063-6294a90aee74			cadae32f-3c14-45d4-979b-ff963067cbab	2025-01-01	Warnings	Exact identifier spl set id: cadae32f-3c14-45d4-979b-ff963067cbab

Reported adverse events (FAERS/openFDA)#

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