Negara: Amerika Serikat
Bahasa: Inggris
Sumber: NLM (National Library of Medicine)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
GOJO Industries, Inc.
BENZALKONIUM CHLORIDE
BENZALKONIUM CHLORIDE 0.00013
TOPICAL
OTC DRUG
Antimicrobial Hand sanitizer to help reduce bacteria on the skin
OTC monograph not final
PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT- BENZALKONIUM CHLORIDE WIPE CLOTH GOJO INDUSTRIES, INC. _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._ ---------- PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT ACTIVE INGREDIENT Benzalkonium Chloride 0.13% ACTIVE INGREDIENT Benzalkonium Chloride 0.13% PURPOSE Antimicrobial USE Hand sanitizer to help reduce bacteria on the skin WARNINGS FOR EXTERNAL USE ONLY WHEN USING THIS PRODUCT do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. STOP USE AND ASK A DOCTOR IF irritation or rash appears and lasts KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away. DIRECTIONS • Wet hands thoroughly with product and allow to dry • Children under 6 years of age should be supervised when using PURELL INACTIVE INGREDIENTS Water (Aqua), Decyl Glucoside, Glycerin, Fragrance(Parfum), Phenoxyethanol PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT benzalkonium chloride wipe cloth PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:21749-359 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZ ALKONIUM CHLORIDE 0.13 mg in 100 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:21749- 359-10 10 in 1 PACKAGE 08/01/2014 1 37 mL in 1 PACKAGE; Type 0: Not a Combination Product 2 NDC:21749- 359-15 15 in 1 PACKAGE 08/01/2014 02/02/2020 2 64 mL in 1 PACKAGE; Type 0: Not a Combination Product 3 NDC:21749- 359-20 20 in 1 PACKAGE 08/01/2014 3 74 mL in 1 PACKAGE; Type 0: Not a Combinati Baca dokumen lengkapnya