Land: USA
Språk: engelska
Källa: NLM (National Library of Medicine)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
Antibacterial Wet Wipes
TOPICAL
OTC DRUG
Antibacterial Wet Wipes For hand sanitizing to decrease bacteria on the skin,kills 99.9% common germs Stop use and ask a doctor if irritation or redness develop
OTC monograph not final
ANTIBACTERIAL WET WIPES- ANTIBACTERIAL WET WIPES CLOTH ANTIBACTERIAL WET WIPES _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._ ---------- 81991-002 ANTIBACTERIAL WIPES Benzalkonium chloride 0.13% Antibacterial Wet Wipes For hand sanitizing to decrease bacteria on the skin,kills 99.9% common germs For external Use only When use this product avoid contact with the eyes.In case of contact, flush eyes thoroughly with water. Stop use and ask a doctor if irritation or redness develop Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away. Directions Take wipe and rub thoroughly over all surfaces of both hands Rub hands together briskly to dry Dispose of wipes Water,Glycerin, Disodium Cocoamphodiacetate, Phenoxyethanol, Benzoic Acid, Polysorbate 20, Potassium Sorbate, Aloe Barbadensis Leaf Juice, Sodium Citrate ANTIBACTERIAL WET WIPES antibacterial wet wipes cloth PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:81991-002 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZ ALKONIUM CHLORIDE 0.13 g in 100 g INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) PHENOXYETHANOL (UNII: HIE492ZZ3T) BENZOIC ACID (UNII: 8SKN0B0MIM) Antibacterial Wet Wipes GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM CITRATE (UNII: 1Q73Q2JULR) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:81991- 002-37 65 in 1 CANISTER 01/06/2022 1 0.0042 g in 1 POUCH; Type 0: Not a Combination Product MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DAT Läs hela dokumentet