FDA.reportPublic FDA data

Ban Purely Gentle

Manufacturer
Kao USA Inc.
Effective date
2025-01-01
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 20:43:24

Label at a glance#

ProductBan Purely Gentle Roll-On Antiperspirant Deodorant Unscented
Active ingredientALUMINUM CHLOROHYDRATE
Label structure14 sections

Storage and handling

Other information store at room temperature

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

©2021 Made in Canada

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ban

purely gentle
non-irritating - unscented

INVISIBLE ROLL-ON

CRUELTY FREE • PARABEN FREE • DYE FREE

antiperspirant deodorant

3.5 FL OZ (103 mL)

10596-402-35-UPDATED10596-402-35-UPDATED

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10596-402BAN PURELY GENTLE ROLL-ON ANTIPERSPIRANT DEODORANT UNSCENTED (ALUMINUM CHLOROHYDRATE) LIQUID [KAO USA INC.]6Legacy NDC20250109_5d08ba4d-87d6-eed5-e053-2991aa0acc7d.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10596-40210596-402-35, 10596-402-14

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
NameUNIIKind
PPG-11 STEARYL ETHERS4G2J0Y0LGIACT
WATER059QF0KO0RIACT
STEARETH-2V56DFE46J5IACT
STEARETH-20L0Q8IK9E08IACT
SANDALWOOD3641YW25N2IACT
PHELLODENDRON AMURENSE BARKPBG27B754GIACT
BARLEY5PWM7YLI7RIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
SUNFLOWER OIL3W1JG795YIIACT

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4744c3a2-bc7f-fffc-e063-6294a90a0bf95d08ba4d-87d6-eed5-e053-2991aa0acc7d2025-12-31WarningsExact identifier
spl set id: 5d08ba4d-87d6-eed5-e053-2991aa0acc7d

Reported adverse events (FAERS/openFDA)#

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