Maa: Yhdysvallat
Kieli: englanti
Lähde: NLM (National Library of Medicine)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
Midway Advanced Products LLC
TOPICAL
OTC DRUG
Antiseptic For handwashing to decrease bacteria on the skin.
OTC monograph not final
B4 ANTISEPTIC HAND SANITIZER BENZALKONIUM CHLORIDE 0.13%- BENZALKONIUM CHLORIDE GEL MIDWAY ADVANCED PRODUCTS LLC REFERENCE LABEL SET ID: F39D7373-1742-49CC-986C-9BB95955B847 _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._ ---------- B4 ANTISEPTIC HAND SANITIZER BENZALKONIUM CHLORIDE GEL 0.13% ACTIVE INGREDIENT Benzalkonium chloride 0.13% PURPOS E Antiseptic US E For handwashing to decrease bacteria on the skin. WARNINGS FOR EXTERNAL USE ONLY DO NOT USE in the eyes STOP USE AND ASK A DOCTOR IF irritation and redness develop if condition persists for more than 72 hours. KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact Poison Control Center right away. DIRECTIONS Wet hands thoroughly with product and allow to dry without wiping OTHER INFORMATION store at room temperature INACTIVE INGREDIENTS butylene glycol, caesalpinia spinosa gum, citric acid, ethylhexylgycerin, fragrance, glycerin, phenoxyethanol, sodium lauryl sulfate, water PACKAGE LABELING: B4 ANTISEPTIC HAND SANITIZER BENZALKONIUM CHLORIDE 0.13% benzalkonium chloride gel Midway Advanced Products LLC PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:5249 0 -50 0 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6 JUD5X6 Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH WATER (UNII: 0 59 QF0 KO0 R) BUTYLENE GLYCO L (UNII: 3XUS8 5K0 RA) GLYCERIN (UNII: PDC6 A3C0 OX) CAESALPINIA SPINO SA RESIN (UNII: WL38 8 3U2PO) SO DIUM LAURYL SULFATE (UNII: 36 8 GB5141J) CITRIC ACID MO NO HYDRATE (UNII: 29 6 8 PHW8 QP) PHENO XYETHANO L (UNII: HIE49 2ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:5249 0 -50 0 -15 15 mL in 1 TUBE; Lue koko asiakirja