Country: United States
Language: English
Source: NLM (National Library of Medicine)
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)
Hangzhou Haorun Technology CO.,LTD.
Benzalkonium Chloride
Benzalkonium Chloride 0.13 g in 100 g
TOPICAL
OTC DRUG
for hand washing to decrease bacteria on skin
OTC monograph not final
ANTIBACTERIAL WET WIPES- BENZALKONIUM CHLORIDE SWAB HANGZHOU HAORUN TECHNOLOGY CO.,LTD. _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._ ---------- ANTIBACTERIAL WET WIPES ACTIVE INGREDIENT Benzalkonium chloride 0.13% PURPOS E Antibacterial US E for hand washing to decrease bacteria on skin WARNINGS For External use only. Do not use if you are allergic to any of the ingredients. When using this product Do not get into eyes,if contact occurs ,rinse throughly with water. Discontinue use if irritation or redness develops if condition persists for more than 72 hours consults a physician. KEEP OUT OF REACH OF CHILDREN keep out of reach of children unless under adult supervision .if seallowed ,get medical help or contact a Poison Control Center immediately. DIRECTIONS Thoroughly wipe hands or face with wipe,Discard in trash receptacle;do not flush.Be sure to reseal label complete to retain moisture INACTIVE INGREDIENTS WATER PROPYLENE GLYCOL OCTHILINONE .ALPHA.-TOCOPHEROL ANTIBACTERIAL WET WIPES benzalkonium chloride swab PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:578 17-10 0 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH BENZA LKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (Benzalko nium - UNII:7N6 JUD5X6 Y) Benzalko nium Chlo ride 0 .13 g in 10 0 g INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH WATER (UNII: 0 59 QF0 KO0 R) PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3) O CTHILINO NE (UNII: 4LFS24GD0 V) .ALPHA.-TO CO PHERO L (UNII: H4N8 55PNZ1) PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:578 17-10 0 -0 1 1 in 1 BOTTLE 1 10 g in 1 POUCH 2 NDC:578 17-10 0 -0 2 2 in 1 BOTTLE 2 8 g in 1 POUCH 3 NDC:578 17-10 0 -0 3 3 in 1 BOTTLE 3 6 g in 1 POUCH 4 NDC:578 17-10 0 -0 4 4 in 1 BOTTLE 4 5 g in 1 POUCH 5 NDC:578 17-10 0 -0 5 5 in 1 BOTTLE 5 5 g in Read the complete document