Label: OPTISOURCE ANTIBACTERIAL FOAM HAND- benzalkonium chloride soap
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Contains inactivated NDC Code(s)
NDC Code(s): 64646-001-02 - Packager: Charlotte Products Ltd.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 4, 2019
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Warnings
- When using
- Stop using and ask doctor if
- Keep out of reach of children.
- Directions
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
OPTISOURCE ANTIBACTERIAL FOAM HAND
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64646-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) COCO GLUCOSIDE (UNII: ICS790225B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64646-001-02 4 in 1 CASE 12/22/2015 1 1250 mL in 1 BOTTLE, DISPENSING; 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 11/03/2015 Labeler - Charlotte Products Ltd. (248293359) Registrant - Charlotte Products Ltd. (248293359) Establishment Name Address ID/FEI Business Operations Charlotte Products Ltd. 248293359 manufacture(64646-001)