FDA.reportPublic FDA data

Ban

Manufacturer
Kao USA Inc.
Effective date
2019-10-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:08:05

Label at a glance#

ProductBan Invisible Solid Antiperspirant Deodorant Simply Clean
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
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 zirconium tetrachlorohydrex gly 19%

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

cyclopentasiloxane, stearyl alcohol, PPG-17, hydrogenated castor oil, C12-15 alkyl benzoate, fragrance, oleic acid, behenyl alcohol, 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.feelbanfresh.com

Dist. by Kao USA Inc. Cincinnati, OH 45214

© 2016 Reg. U.S. Pat. and Tm. Off.

Made in Canada

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ban®

simply clean
INVISIBLE SOLID

ANTIPERSPIRANT DEODORANT

2.6 OZ. (73 g)

10596-401-2610596-401-26

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10596-40110596-401-26

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOMETHICONE 50THT5PCI0RIACT
PPG-17OV0Q322E0UIACT
SUNFLOWER OIL3W1JG795YIIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
PHELLODENDRON AMURENSE BARKPBG27B754GIACT
OLEIC ACID2UMI9U37CPIACT
SANDALWOOD3641YW25N2IACT
DOCOSANOL9G1OE216XYIACT
BARLEY5PWM7YLI7RIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
STEARYL ALCOHOL2KR89I4H1YIACT

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
bda7ce9d-e155-9fbd-e053-2995a90aaccc34dc8c79-45e4-7448-e054-00144ff88e882021-03-16WarningsExact identifier
spl set id: 34dc8c79-45e4-7448-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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