Susan Lucci Youthful Essence Daily Protection Moisturizer Sunscreen SPF 15 description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Susan Lucci Youthful Essence Daily Protection Moisturizer Sunscreen SPF 15

Guthy-Renker LLC

Youthful Essence Daily Protection Moisturizer Sunscreen SPF 15


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active Ingredient Purpose
Octinoxate 7.5%
Octisalate 5.0%
Oxybenzone 2.0% Sunscreen

Use

Helps prevent sunburn. Higher SPF gives more sunburn protection.

Warning

For external use only.

When using this product keep out of eyes. Rinse with water to remove. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if rash and irritation develops and lasts.

Keep out of reach of children.

Directions

Apply liberally before sun exposure and as needed. Children under 6 months of age: ask a doctor.

Inactive Ingredients

Water (Eau), Isohexadecane, Propylene Glycol, Ethylhexyl Stearate, Potassium Cetyl Phosphate, Stearic Acid, Glyceryl Stearate, Alteromonas Ferment Extract, Anthemis Nobilis Flower Extract, Avena Sativa (Oat) kernel Extract, Centella Asiatica Extract, Cola Acuminata Seed Extract, Imperala Cylindrica Root Extract, Tilia Cordata Flower Extract, Butyrospermum Parkii (Shea Butter), Hydrolyzed Oats, Butylene Glycol, Dimethicone, Glycerin, Caprylyl Glycol, Sucrose Cocoate, Sorbitan Stearate, Cetyl Alcohol, Sclerotium Gum, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Tetrasodium EDTA, Butylparaben, Ethylparaben, Propylparaben, Isobutylparaben, Methylparaben, Phenoxyethanol, Potassium Sorbate, Fragrance (Parfum)

PRINCIPAL DISPLAY PANEL - 15mL Label

Daily Protection Moisturizer Sunscreen
SPF 15

e 15mL 0.5 FL OZ

Susan Lucci Youthful Essence Daily Protection Moisturizer Sunscreen SPF 15

Susan Lucci Youthful Essence Daily Protection Moisturizer Sunscreen SPF 15

OCTINOXATE, OCTISALATE, and OXYBENZONE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11410-810
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 7.5 mg
OCTISALATE OCTISALATE 5 mg
OXYBENZONE OXYBENZONE 2 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11410-810-07 15 in 1 JAR
2 NDC:11410-810-19 50 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2008-06-01


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.