Country: Bandaríkin
Tungumál: enska
Heimild: NLM (National Library of Medicine)
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
PureTek Corporation
Benzalkonium Chloride
Benzalkonium Chloride 1.3 mg in 1 mL
OTC DRUG
OTC monograph not final
GENRX ALL PURPOSE CLEANSING- BENZALKONIUM CHLORIDE SPRAY PURETEK CORPORATION _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._ ---------- ACTIVE INGREDIENT Benzalkonium Chloride 0.13% PURPOS E Antiseptic US ES ■ a no-rinse topical antiseptic that protects against bacterial contamination WARNINGS FOR EXTERNAL USE ONLY DO NOT USE ON ■ deep or puncture wounds ■ animal bites ■ serious burns WHEN USING THIS PRODUCT ■ do not get into eyes STOP USE AND ASK A DOCTOR IF ■ condition worsens ■ symptoms last more than 7 days or clear up and occur again within a few days KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away. DIRECTIONS ■ spray soiled and/or odorous (body and/or perineal) areas ■ gently wipe clean ■ repeat as necessary until all soils are removed and skin is clean ■ pat dry (no rinsing necessary) ■ apply GenRx protectant cream or paste as necessary OTHER INFORMATION ■ protect from freezing ■ avoid excessive heat INACTIVE INGREDIENTS _Aloe barbadensis_ (_Aloe vera_) leaf juice, butylene glycol, disodium EDTA, fragrance, glycerin, GenRx Complex™ [consisting of: bisabolol, calcium pantothenate (vitamin B ), _Carthamus tinctorius_ 5 (safflower) oleosomes, maltodextrin, niacinamide (vitamin B ), pyridoxine HCl (vitamin B ), silica, sodium ascorbyl phosphate (vitamin C), sodium starch octenylsuccinate, tocopheryl acetate (vitamin E), _Zingiber officinale_ (ginger) root extract], phenoxyethanol, polysorbate 20, purified water, sodium hyaluronate, sodium hydroxide. GENRX ALL PURPOSE CLEANSING SPRAY (8 OZ LABEL) GENRX ALL PURPOSE CLEANSING benzalkonium chloride spray PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:59 0 8 8 -543 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH BENZA LKO NIUM CHLO R Lestu allt skjalið