Label: BAN ROLL-ON ANTIPERSPIRANT DEODORANT UNSCENTED- aluminum chlorohydrate liquid
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NDC Code(s):
10596-338-11,
10596-338-14,
10596-338-15,
10596-338-35, view more10596-338-70
- Packager: Kao USA Inc.
- Category: HUMAN OTC DRUG LABEL
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
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- 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
- CANADA MFD LABEL
- USA MANUFACTURED LABEL
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INGREDIENTS AND APPEARANCE
BAN ROLL-ON ANTIPERSPIRANT DEODORANT UNSCENTED
aluminum chlorohydrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10596-338 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) PPG-11 STEARYL ETHER (UNII: S4G2J0Y0LG) SUNFLOWER OIL (UNII: 3W1JG795YI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10596-338-35 103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 01/01/2012 2 NDC:10596-338-70 2 in 1 PACKAGE 09/12/2016 2 103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 3 NDC:10596-338-15 44 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 11/04/2016 4 NDC:10596-338-11 3 in 1 PACKAGE 06/23/2020 4 103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 5 NDC:10596-338-14 4 in 1 PACKAGE 08/24/2020 5 103 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 M026 01/01/2012 Labeler - Kao USA Inc. (004251617)