BAN ROLL-ON ANTIPERSPIRANT DEODORANT REGULAR- aluminum chlorohydrate liquid

Ban by

Drug Labeling and Warnings

Ban by is a Otc medication manufactured, distributed, or labeled by Kao USA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Aluminum chlorohydrate 18%

PURPOSE

Purpose

Antiperspirant

INDICATIONS & USAGE

Use

reduces underarm perspiration

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use on broken skin

STOP USE

Stop use if rash or irritation occurs

ASK DOCTOR

Ask a doctor before use if you have kidney disease

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

apply to underarms only

STORAGE AND HANDLING

Other information

store at room temperature

INACTIVE INGREDIENT

Inactive ingredients

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

SPL UNCLASSIFIED SECTION

Questions? 1-866-226-3363

www.feelbanfresh.com

BAN is a trademark of Kao Corp.

Dist. by Kao USA Inc. Cincinnati, OH 45214

©2017 Made in Canada

PRINCIPAL DISPLAY PANEL

ban

regular

ROLL-ON

ANTIPERSPIRANT·DEODORANT

1.5 FL OZ (44 mL)

INGREDIENTS AND APPEARANCE

BAN  ROLL-ON ANTIPERSPIRANT DEODORANT REGULAR
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10596-336
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	20 g  in 103 mL

Inactive Ingredients
Ingredient Name	Strength
PPG-11 STEARYL ETHER (UNII: S4G2J0Y0LG)
WATER (UNII: 059QF0KO0R)
STEARETH-2 (UNII: V56DFE46J5)
STEARETH-20 (UNII: L0Q8IK9E08)
SANDALWOOD (UNII: 3641YW25N2)
PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
BARLEY (UNII: 5PWM7YLI7R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SUNFLOWER OIL (UNII: 3W1JG795YI)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10596-336-35	103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/01/2012
2	NDC: 10596-336-70	2 in 1 PACKAGE	09/12/2016
2		103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
3	NDC: 10596-336-15	44 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/04/2016
4	NDC: 10596-336-14	4 in 1 PACKAGE	12/12/2019
4		103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/01/2012

Labeler - Kao USA Inc. (004251617)