Држава: Сједињене Америчке Државе
Језик: Енглески
Извор: NLM (National Library of Medicine)
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
Navajo Manufacturing Company Inc.
TOPICAL
OTC DRUG
- Hand sanitized to help reduce bacteria on the skin
OTC monograph not final
PURELL- ALCOHOL GEL NAVAJO MANUFACTURING COMPANY INC. ---------- PURELL _DRUG FACTS_ _ACTIVE INGREDIENT _ Ethyl Alcohol 70% v/v _PURPOSE_ _USES_ Hand sanitized 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_ Put enough product in your palm to cover hands and rub hands together briskly until dry Children under 6 years of age should be supervised when using this product _OTHER INFORMATION_ Store below 110°F (43°C) May discolor certain fabrics or surfaces Antimicrobial _INACTIVE INGREDIENTS_ Water (Aqua), Isopropyl Alcohol, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30, Alkly Acrylate, Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum) _QUESTIONS?_ 1-888-4-PURELL WWW.PURELL.COM PURELL, 1OZ PURELL, 2OZ PURELL alcohol gel PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:67751-188(NDC:21749-704) ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Navajo Manufacturing Company Inc. INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:67751-188- 01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/04/2017 2 NDC:67751-188- 02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/04/2017 09/01/2021 MARKETING INFORMATION MARKETING CATEGORY AP Прочитајте комплетан документ