Susan Lucci Youthful Essence Daily Protection Moisturizer Sunscreen SPF 15

Dosage form: cream
Ingredients: OCTINOXATE 7.5mg in 100mL, OCTISALATE 5mg in 100mL, OXYBENZONE 2mg in 100mL
Labeler: Guthy-Renker LLC
NDC Code: 11410-810

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Youthful Essence Daily Protection
Moisturizer Sunscreen SPF 15

Drug Facts

Active IngredientPurpose
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 
octinoxate, octisalate, and oxybenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11410-810
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE7.5 mg  in 100 mL
OCTISALATE (OCTISALATE) OCTISALATE5 mg  in 100 mL
OXYBENZONE (OXYBENZONE) OXYBENZONE2 mg  in 100 mL
Packaging
#Item CodePackage Description
1NDC:11410-810-0715 mL in 1 JAR
2NDC:11410-810-1950 mL in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35206/01/2008
Labeler - Guthy-Renker LLC (608315453)

Revised: 06/2010
 
Guthy-Renker LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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