Label: BAN ROLL-ON ANTIPERSPIRANT DEODORANT SATIN BREEZE- aluminum chlorohydrate liquid
- NDC Code(s): 10596-339-14, 10596-339-35, 10596-339-70
- Packager: Kao USA Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 28, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- STOP USE
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BAN ROLL-ON ANTIPERSPIRANT DEODORANT SATIN BREEZE
aluminum chlorohydrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10596-339 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 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) PPG-11 STEARYL ETHER (UNII: S4G2J0Y0LG) SUNFLOWER OIL (UNII: 3W1JG795YI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10596-339-35 103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 01/01/2012 2 NDC:10596-339-14 4 in 1 PACKAGE 08/24/2020 2 103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 3 NDC:10596-339-70 2 in 1 PACKAGE 08/24/2020 3 103 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)