Solbar Avo SPF35 description, usages, side effects, indications, overdosage, supplying and lots more!

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Solbar Avo SPF35

Person and Covey

Solbar Avo SPF35


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Indications and use

Helps prevent sunburn. If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun. Dosage and Administration: Apply liberally and evenly to all sun exposed areas of DRY skin 15 minutes before sun exposure. Reapply after 80 minutes of swimming or sweating and immediately after towel drying. Apply at least every 2 hours. For children under 6 months, ask a physician.

Purpose

Sunscreen

Keep out of the reach of children

Yes. If swallowed, get medical help or contact a Poison Control Center right away.

Dosage and Administration

Apply liberally and evenly to all sun exposed areas of DRY skin 15 minutes before sun exposure. Reapply after 80 minutes of swimming or sweating and immediately after towel drying. Apply at least every 2 hours. For children under 6 months, ask a physician.

Warnings

For external use only. Do not use on damaged or broken skin. Keep out of eyes. Rinse eyes thoroughly with water to remove. Stop use and ask a physician if rash or irritation develops and lasts. Store away from excessive heat and direct sun.

OTC - ACTIVE INGREDIENT SECTION

Homosalate

Octinoxate

Oxybenzone

Avobenzone

INACTIVE INGREDIENT SECTION

Water

Isobutyl Stearate

Glycerin

Benzyl Alcohol

Simethicone

Cetyl Phosphate

Triethanolamine

Stearic Acid

Silica

Carbomer 1342

Acrylates/C10-30 Alkyl Acrylate Crosspolymer

Disodium EDTA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

solbar avo.jpgSolbar Avo SPF35

Solbar Avo SPF35

Solbar Avo SPF35 CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0096-0687
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HOMOSALATE Homosalate 0.08 g
OCTINOXATE OCTINOXATE 0.075 g
OXYBENZONE OXYBENZONE 0.06 g
AVOBENZONE AVOBENZONE 0.03 g

Inactive Ingredients

Ingredient Name Strength
water
ISOBUTYL STEARATE
GLYCERIN
BENZYL ALCOHOL
CETYL PHOSPHATE
TROLAMINE
STEARIC ACID
SILICON DIOXIDE
CARBOMER 1342
(C10-C30)ALKYL METHACRYLATE ESTER
EDETATE DISODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0096-0687-04 119 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 1996-06-01


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