Solbar Zinc SPF38 description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Solbar Zinc SPF38

Person and Covey

Solbar Zinc


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Indications and use

Helps prevent sunburn.

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

Zinc Oxide

INACTIVE INGREDIENT SECTION

Water

Isobutyl Stearate

PEG-100 Stearate

Glycerin

Dimethicone

PVP/Eicosene Copolymer

Glyceryl Dilaurate

Cetyl Alcohol

DEA Cetyl Phosphate

Benzyl Alcohol

Cyclomethicone

Stearyl Alcohol

Xanthan Gum

Disodium EDTA

Citric Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Solbar Zinc.jpgSolbar Zinc SPF38

Solbar Zinc SPF38

Solbar Zinc SPF38 CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0096-0688
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HOMOSALATE Homosalate 0.1015 1
OCTINOXATE OCTINOXATE 0.077 1
Zinc Oxide Zinc oxide 0.077 1

Inactive Ingredients

Ingredient Name Strength
water
ISOBUTYL STEARATE
PEG-100 STEARATE
GLYCERIN
DIMETHICONE
EICOSYL POVIDONE (2 EICOSYL BRANCHES/REPEAT)
GLYCERYL DILAURATE
CETYL ALCOHOL
DIETHANOLAMINE CETYL PHOSPHATE
BENZYL ALCOHOL
cyclomethicone
stearyl alcohol
XANTHAN GUM
EDETATE SODIUM
ANHYDROUS CITRIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0096-0688-04 115.0 in 1 BOTTLE

Marketing Information

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


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.