AVERTEAX description, usages, side effects, indications, overdosage, supplying and lots more!

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AVERTEAX

Camellix, LLC

AVERTEX Benzyl Alcohol


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

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

AVERTEAX

AVERTEAX

Benzyl Alcohol CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54866-002
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZYL ALCOHOL 10 mg

Inactive Ingredients

Ingredient Name Strength
water
CARBOMER COPOLYMER TYPE A
CETYL ALCOHOL
STEARIC ACID
GLYCOL STEARATE
GLYCERYL MONOSTEARATE
SAFFLOWER OIL
propylene glycol
GLYCERIN
DIMETHICONE
PHENOXYETHANOL
Aloe Vera Leaf
EPIGALLOCATECHIN GALLATE STEARATES
EPIGALLOCATECHIN GALLATE PALMITATES
EUCALYPTUS OIL
HYALURONIC ACID
LUTEIN
CALENDULA OFFICINALIS FLOWER
TROLAMINE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 7.4 in 1 TUBE
2 NDC:54866-002-01 1 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-01-01


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Be sure to consult your doctor before taking any medication!
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