Country: United States
Language: English
Source: NLM (National Library of Medicine)
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)
Kimberly-Clark
TOPICAL
OTC DRUG
Antiseptic cleanser For personal hand hygiene to help prevent the spread of bacteria
OTC monograph not final
KLEENEX FOAM HAND SANITIZER- BENZALKONIUM CHLORIDE SOLUTION KIMBERLY-CLARK _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._ ---------- KLEENEX FOAM HAND SANITIZER DRUG FACTS ACTIVE INGREDIENT Benzalkonium Chloride 0.13%w/w PURPOSE Antiseptic cleanser USE For personal hand hygiene to help prevent the spread of bacteria WARNINGS FOR EXTERNAL USE ONLY. Do not ingest. Use with caution in children. DO NOT USE if you are allergic to any ingredients. WHEN USING THIS PRODUCT, avoid contact with eyes. If contact occurs, rinse with water. STOP USE AND ASK A DOCTOR IF irritation develops. KEEP OUT OF REACH OF CHILDREN. If swallowed, call a poison control centre or get medical help right away. DIRECTIONS Apply small amount and rub thoroughly into hands for at least 30 seconds. Allow to dry. Not to be rinsed off with water (i.e. not to be used as a handwash). For occasional and personal domestic use. Supervise children when they use this product. OTHER INFORMATION Report serious side effects from this product to 1-877-561-6587. ® INACTIVE INGREDIENTS Aloe Barbadensis Leaf Juice Powder, Citric Acid, Cocamidopropyl PG-Dimonium Chloride Phosphate, Methylpropanediol, Panthenol, PEG-14M, Silica, Sodium Hydroxide, Water QUESTIONS? 1-888-346-4652 Distributed in the U.S. by Kimberly-Clark Global Sales, LLC, Roswell, GA 30076-2199 Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5 PRINCIPAL DISPLAY PANEL - 532 ML BOTTLE LABEL Kleenex Foam Hand Sanitizer alcohol free DIN: 02443252 For Personal / Domestic Use Only 18 fl oz (532 mL) ® KLEENEX FOAM HAND SANITIZER benzalkonium chloride solution PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:55118-701 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benz Read the complete document