Label: FOAMING ANTIBACTERIAL HANDSOAP- benzalkonium chloride liquid
- NDC Code(s): 68041-512-01, 68041-512-55
- Packager: Chemcor Chemical Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 26, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive Ingredients
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SPL UNCLASSIFIED SECTION
moisturizes
hard on germs
tough on surface bacteriaCHEMCOR
CHEMICAL CORP
CHINO, CA 91710
CHEMCORCHEMICAL.COM
WARNING
Keep out of reach of children.
May be harmful if swallowed.
May cause irritation to eyes.institutional & commercial antibacterial hand cleanser
DESCRIPTION
An effective antibacterial foaming hand and skin cleanser which contains benzalkonium chloride, an outstanding germ fighter. Formulated to be tough on bacteria and germs. Regular use of this antibacterial handsoap decreases bacteria levels on the skin and helps reduce risk of infection. Produces rich moisturizing lather to promote complete gentle cleansing. Leaves the skin clean, soft and refreshed. May be used in all types of foaming dispensing units.Before discarding container, rinse with water.
For institutional and commercial use.
Antes de descargar el contenedor, enjuague con agua.
Para uso institucional y comercial. - Antibacterial Foaming Handsoap
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INGREDIENTS AND APPEARANCE
FOAMING ANTIBACTERIAL HANDSOAP
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68041-512 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.0013 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERIN (UNII: PDC6A3C0OX) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) MAGNESIUM NITRATE (UNII: 77CBG3UN78) MALTODEXTRIN (UNII: 7CVR7L4A2D) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 40 (UNII: WZB9127XOA) EDETATE SODIUM (UNII: MP1J8420LU) WATER (UNII: 059QF0KO0R) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Product Characteristics Color orange Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68041-512-01 3780 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/15/2020 2 NDC:68041-512-55 207900 mL in 1 DRUM; Type 0: Not a Combination Product 07/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/15/2020 Labeler - Chemcor Chemical Corporation (018129978) Establishment Name Address ID/FEI Business Operations Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. 028311595 manufacture(68041-512) , api manufacture(68041-512) , pack(68041-512)
