Label: CARROLL ULTREX ANTIMICROBIAL WIPES- benzalkonium chloride cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 10685-681-97 - Packager: Carroll Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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Drug Label Information
Updated January 31, 2018
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 70 Cloth Canister Label WIPES CARROLL® ULTREX Antimicrobial Wipes -Kills 99.9% of common germs -Contains Aloe and Vitamin E -Moisturizes and conditions skin -Alcohol free CITRUS SCENTED Dual Textured Wipe KEEP OUT OF REACH OF CHILDREN WARNING For external use only. Contains 70 12" x 10" Pre-Moistened Wipes ITEM # 681
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INGREDIENTS AND APPEARANCE
CARROLL ULTREX ANTIMICROBIAL WIPES
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10685-681 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.01417 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) EDETATE SODIUM (UNII: MP1J8420LU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10685-681-97 70 in 1 CANISTER; Type 0: Not a Combination Product 09/15/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 09/15/2012 Labeler - Carroll Company (007372329) Registrant - Carroll Company (007372329) Establishment Name Address ID/FEI Business Operations Carroll Company 007372329 manufacture(10685-681)