Valsts: Amerikas Savienotās Valstis
Valoda: angļu
Klimata pārmaiņas: NLM (National Library of Medicine)
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
S.P. Richards Company
Alcohol
Alcohol .62 mL in 1 mL
TOPICAL
OTC DRUG
Antiseptic - to decrease bacteria on the skin that could cause disease - recommended for repeated use - irritation and redness develop - condition persists for more than 72 hours
OTC monograph not final
ETHYL ALCOHOL- ETHYL ALCOHOL LOTION S.P. RICHARDS COMPANY _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._ ---------- GENUINE JOE 447.001-447AC MOISTURIZING FOAMING HAND SANITIZER FF ACTIVE INGREDIENT Ethyl alcohol 62% PURPOSE Antiseptic USES to decrease bacteria on the skin that could cause disease recommended for repeated use WARNINGS FOR EXTERNAL USE ONLY: HANDS FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME. WHEN USING THIS PRODUCT Keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin do not inhale or ingest STOP USE AND ASK A DOCTOR IF irritation and redness develop condition persists for more than 72 hours 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 without wiping for children under 6, use only under adult supervision not recommended for infants OTHER INFORMATION do not store above 105°F may discolor some fabrics harmful to wood finishes and plastics INACTIVE INGREDIENTS water, PEG-8 dimethicone, meadowfoamamidopropyl betaine, glycerin, tocopheryl acetate, isopropyl myristate Distributed by: S.P. Richards Company, Smyrna, GA 30082 www.genuinejoe.com SDS-MO-15036 SDA-WI-2486 DSP-MO-28 DSP-MO-34 447.001/447AC PRINCIPAL DISPLAY PANEL Genuine Joe MOISTURIZING FOAMING HAND SANITIZER Fragrance Free 10453 8 FL OZ (236 mL) ETHYL ALCOHOL ethyl alcohol lotion PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:62832-447 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol .62 mL in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) PEG-8 DIMETHICONE (UNII: GIA7T764OD) MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG) GLYCERIN (UNI Izlasiet visu dokumentu