Label: HAND WASH- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 57243-641-96 - Packager: Salado Sales, Inc
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated July 21, 2017
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- Active ingredient
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- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
HAND WASH
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57243-641 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE .999 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) COCO MONOETHANOLAMIDE (UNII: C80684146D) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE SODIUM (UNII: MP1J8420LU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 4 (UNII: X3W0AM1JLX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57243-641-96 221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/04/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/04/2014 Labeler - Salado Sales, Inc (009830555) Registrant - Vi-Jon (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon 088520668 manufacture(57243-641)