Label: PERSONAL CARE ANTIBACTERIAL FOAMING HAND WILD FLOWERS- benzalkonium chloride liquid
PERSONAL CARE ANTIBACTERIAL FOAMING HAND FRESH PICKED STRAWBERRIES- benzalkonium chloride liquid
PERSONAL CARE ANTIBACTERIAL FOAMING HAND BEACH BREEZE- benzalkonium chloride liquid
PERSONAL CARE ANTIBACTERIAL FOAMING HAND CITRUS SUNSHINE- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 29500-9018-1, 29500-9020-1, 29500-9319-1, 29500-9881-1 - Packager: Personal Care Products, LLC
- 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 December 10, 2015
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug FactsActive ingredient
- Purpose
- Keep out of reach of children
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor
- Directions
- Inactive ingredients
- Personal CARE ® ANTIBACTERIAL FOAMING Hand Soap LabelsWild FlowersFresh Picked StrawberriesBreach BreezeCitrus Sunshine
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INGREDIENTS AND APPEARANCE
PERSONAL CARE ANTIBACTERIAL FOAMING HAND WILD FLOWERS
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:29500-9881 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.0002218 mg in 221.8 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAURETH-9 (UNII: 0AWH8BFG9A) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:29500-9881-1 221.8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/10/2015 PERSONAL CARE ANTIBACTERIAL FOAMING HAND FRESH PICKED STRAWBERRIES
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:29500-9018 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.0002218 mg in 221.8 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAURETH-9 (UNII: 0AWH8BFG9A) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:29500-9018-1 221.8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/10/2015 PERSONAL CARE ANTIBACTERIAL FOAMING HAND BEACH BREEZE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:29500-9020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.0002218 mg in 221.8 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAURETH-9 (UNII: 0AWH8BFG9A) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:29500-9020-1 221.8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/10/2015 PERSONAL CARE ANTIBACTERIAL FOAMING HAND CITRUS SUNSHINE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:29500-9319 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.0002218 mg in 221.8 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAURETH-9 (UNII: 0AWH8BFG9A) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:29500-9319-1 221.8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/10/2015 Labeler - Personal Care Products, LLC (966155082) Registrant - Personal Care Products, LLC (966155082)