Avertex Benzyl Alcohol ⮝
Active ingredient Purpose
Benzyl Alcohol (1.0%) Cold Sores & Fever blisters
Purpose: ⮝
Treats cold sores and fever blisters, a vesicle that occurs at the junction of the mucous membrane and the skin on the lips or nose and is caused by the virus herpes simplex, type 1.
Ask Doctor: ⮝
If condition worsens or does not improve after regular use of the product as directed, consult a doctor.
If swallowed, contact a doctor.
Warnings: ⮝
For external use only.
Directions: ⮝
For the temporary relief of pain and itching of cold sores and fever blisters, apply AverTeaX ointment directly on the affected area throughout the day as needed. To achieve best result, apply at the frist sign of symptons (redness, tingling, tightness, or itching.)
Stop Use: ⮝
If illergic to any ingridient of the product.
Indications & Usage: ⮝
Indications are for pain and itching associated with fever blisters and cold sores.
For the temporary Relief of Pain and itching associated with fever blisters and cold sores.
Do Not Use: ⮝
If allergic to any ingredient of the product.
Keep Out Of Reach Of Children: ⮝
- Keep out of reach of children.
- If swallowed, contact a doctor.
Inactive Ingredient ⮝
Ultrez 10 (Carbopol), Cetyl Alcohol (Powder Form), Stearic Acid, E. Glycol Stearate (EGMS), Glyceryl Stearate (GMS), Safflower Oil, Propylene Glycol USP, Glycerin (USP Grade) 99.7%, PMX-200 Silicone Fluid, Euxyl PE 9010 (0.5% - 1.0%), Aloe Vera, EGCG (Epigallocatechin-3-Gallate, Extracted from Green Tea) Stearate, EGCG Palmitate, Eucalyptus oil, Sodium Hyaluronate (Hyaluronic Acid), Lutein 10% (Marigold Ext. 10%), TEA (Triethanolamine)(99%).
AVERTEAX TOPICAL OINTMENT COLD SORES AND FEVER BLISTERS TREATMENT DISTRIBUTED BY CAMELLIX MADE IN USA
Principal Display Panal ⮝
AVERTEAX
benzyl alcohol cream
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54866-002 Route of Administration TOPICAL
Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH) BENZYL ALCOHOL 10 mg in 1 g
Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) CETYL ALCOHOL (UNII: 936JST6JCN) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCOL STEARATE (UNII: 0324G66D0E) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) Safflower Oil (UNII: 65UEH262IS) Propylene Glycol (UNII: 6DC9Q167V3) Glycerin (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALOE VERA LEAF (UNII: ZY81Z83H0X) EPIGALLOCATECHIN GALLATE STEARATES (UNII: MGB2NQG22C) EPIGALLOCATECHIN GALLATE PALMITATES (UNII: M213AC47MB) EUCALYPTUS OIL (UNII: 2R04ONI662) Hyaluronic Acid (UNII: S270N0TRQY) LUTEIN (UNII: X72A60C9MT) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) TROLAMINE (UNII: 9O3K93S3TK)
Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54866-002-01 1 in 1 PACKAGE 1 7.4 g in 1 TUBE
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 01/01/2014
Labeler - Camellix, LLC (968429386)
Establishment Name Address ID/FEI Business Operations Star Health and Beauty, LLC 013506838 manufacture(54866-002) Revised: 3/2014 Document Id: dea0cd6a-9743-4539-a694-c88cf3543525 Set id: f86b5de9-8e44-4d06-890e-75f7e71c79e4 Version: 1 Effective Time: 20140307 Camellix, LLC
