Země: Spojené státy
Jazyk: angličtina
Zdroj: NLM (National Library of Medicine)
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
GOJO Industries, Inc.
TOPICAL
OTC DRUG
Antimicrobial - Hand sanitizer to help reduce bacteria on the skin
OTC monograph not final
PURELL PROFESSIONAL ADVANCED HAND SANITIZER GEL- ALCOHOL GEL 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 PROFESSIONAL ADVANCED HAND SANITIZER GEL ACTIVE INGREDIENT Ethyl alcohol 70% v/v PURPOSE Antimicrobial USES Hand sanitizer to help reduce bacteria on the skin WARNINGS FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME. 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 Place product on hands Rub until dry INACTIVE INGREDIENTS Water (Aqua), Isopropyl Alcohol, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum) PURELL PROFESSIONAL ADVANCED HAND SANITIZER GEL alcohol gel PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:21749-715 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) GOJO Industries, Inc. CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:21749- 715-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/15/2017 2 NDC:21749- 715-12 354 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/15/2017 3 NDC:21749- 715-10 1000 mL in 1 BOTTLE; Type 0: Not a Combinatio Přečtěte si celý dokument