Country: Stati Uniti
Lingwa: Ingliż
Sors: NLM (National Library of Medicine)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
Dolgencorp, LLC
BENZALKONIUM CHLORIDE
BENZALKONIUM CHLORIDE 0.1 g in 100 g
CUTANEOUS
OTC DRUG
Purpose Antibacterial Use For washing to decrease bacteria on the skin. Stop use and ask a doctor if - irritation or redness develops.
OTC monograph not final
BODY BAR GOLD- BENZALKONIUM CHLORIDE SOAP DOLGENCORP, LLC _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._ ---------- DG BODY BAR SOAP GOLD _DRUG FACTS_ _ACTIVE INGREDIENT_ Benzalkonium Chloride 0.1% _PURPOSE_ Antibacterial _USE_ For washing to decrease bacteria on the skin. _WARNINGS_ FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT avoid contact with the eyes. In case of eye contact, flush with water. STOP USE AND ASK A DOCTOR IF irritation or redness develops. KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away. _DIRECTIONS_ Wet bar with water Lather vigorously and wash skin Rinse and dry thoroughly _INACTIVE INGREDIENTS _Sodium Palmate, Water, Sodium Palm Kernelate, Glycerin, Zea Mays (Corn) Starch, Fragrance, Sodium Chloride, Sodium Laureth Sulfate, Etidronic Acid, Tetrasodium EDTA, FD&C Yellow No. 5, FD&C Red No. 4. *This product is not manufactured or distributed by The Dial Corporation, a Henkel Company, owner of the registered trademark Dial®. DISTRIBUTED BY DOLGENCORP, LLC 100 MISSION RIDGE GOODLETTSVILLE, TN 37072 MADE IN COLUMBIA 100% Satisfaction Guaranteed (888) 309-9030 DG body BODY BAR SOAP GOLD BODY BAR SOAP GOLD Antibacterial / Deodorant Gold formula protects from germs and odors Rich, creamy lather Clean-rinsing formula Compare to active ingredient of Dial® Gold® 2 BARS 2-3.5 OZ SOAP BARS (99 G) TOTAL NET WT 7 OZ (198 G) BODY BAR GOLD benzalkonium chloride soap PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:559 10 -20 2 ROUTE OF ADMINISTRATION CUTANEOUS 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 0 .1 g in 10 0 g INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH WATER (UNII: 0 59 QF0 KO0 R) SO DIUM PALMATE (UNII: S0 A6 0 0 4K3Z Aqra d-dokument sħiħ