- DRUG FACTSActive Ingredient
- Purpose
- Keep out of reach of children
- Uses:
- Warnings:
- Directions:
-
Other Ingredients:
Behentrimonium Methosulfate, Bisabolol, Butylene Glycol, Cetyl Alcohol, Chamomilla (Matricaria Recutita) Extract, Chlorhexidine Gluconate, Dimethicone, Mentha Spicata (Spearmint) Oil, Menthyl Lactate, Octyldodecanol, Phenoxyethanol, Polyquaternium,-37, Rosemary(Rosmarinus Officinalis) Leaf Oil, Stearic Acid, Water (Aqua), Witch Hazel (Hamamelis Virginiana) Extract.
- Questions or Comments?Other:
-
QuickMend product label
QUICKMEND
FOR
COLD SORE RELIEF
GET COOL QUICK RELIEF
Symptoms of cold sores relieved QUICKLY.
Use immediately when irritation starts.
Patented formula for QUICK soothing results from cold sores and fever blisters. Treat it as soon as you feel it + get cool QUICK relief!
NEW
CONVIENT PUMP DISPENSER
*as always results may vary. US Patent #8,603,550 9ml/.30 oz.
Lot 000000
Exp. 01/19
GETQUICKMEND.COM Made in the USA. * As always, results may vary
-
INGREDIENTS AND APPEARANCE
QUICKMEND
benzethonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53228-230 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.09 mg in 9 mL Inactive Ingredients Ingredient Name Strength BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61) LEVOMENOL (UNII: 24WE03BX2T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CETYL ALCOHOL (UNII: 936JST6JCN) CHAMOMILE (UNII: FGL3685T2X) CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) DIMETHICONE (UNII: 92RU3N3Y1O) SPEARMINT (UNII: J7I2T6IV1N) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) OCTYLDODECANOL (UNII: 461N1O614Y) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYQUATERNIUM 37 (200 MPA.S) (UNII: 67C1D6YV24) ROSEMARY OIL (UNII: 8LGU7VM393) STEARIC ACID (UNII: 4ELV7Z65AP) WATER (UNII: 059QF0KO0R) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53228-230-01 9 mL in 1 CONTAINER; Type 0: Not a Combination Product 04/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/01/2016 Labeler - Equibal, Inc. (144679883) Registrant - Equibal, Inc. (144679883) Establishment Name Address ID/FEI Business Operations Equibal, Inc. 144679883 manufacture(53228-230)