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SUN Tinted Solar Defense Organic SPF 30

Medically reviewed on July 3, 2017.

Dosage form: cream
Ingredients: ZINC OXIDE 170mg in 1mL
Labeler: Allure Labs, Inc.
NDC Code: 62742-4041

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.

Drug Facts


A physical organic UVA/UVB broad spectrum daily moisturizer. Provides an even skin tone and healthy glow. Ultimate protection against the aging effects of the sun and other environmental pollutants. Enriched with essential vitamins and anti-oxidants that prevent free facical damage. Preserves skin hydration for the entire day.

Paraben Free

Provides Healthy even glow

Excellent for sensitive skin

Chemical free

Water resistant


Apply liberally 15-30 minutes prior to sun exposure or as needed for a even skin tone. Reapply regulary or after prolonged swimming or activity.


Sensitive skin, Sun exposure, uneven skin tone

Active Ingredients:

Zinc Oxide 17%

Inactive Ingredients:

Water (Aqua), Butylene Glycol, Glycerin, Caprylic/Capric Triglyceride, Glyceryl Stearate, PEG 100 Stearate, Sorbitan Stearate, Imperata Cylindrica Root Extract, Phenoxyethanol, Tocophery Linoleate, Ascorbyl Palmitate (Vitamin C), Lecithin, Tocopherol (Vitamin E), Xanthan Gum, Citric Acid, C13-14 Isoparaffin, PEG 8, Ethylhexylglycerin, Sodium Lactate, Micrococcus Lysate, Arabidopsis Extract, Plankton Extract, Teprenone, Phoenix dactylifera (date) Extract, Laureth-7, Disodium EDTA, Dipotassium Glycyrrizate, Caprylyl Glycol, Ascorbic Acid (Viamin C), Carbomer, Iron Oxides (CL 72124, Cl 7212 and Cl72123)


Image International

Palm Beach, FL 33411 USA

Image of the Product:

SUN Tinted Solar Defense Organic SPF 30

zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4041
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
#Item CodePackage Description
1NDC:62742-4041-156.7 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35201/01/2010
Labeler - Allure Labs, Inc. (926831603)

Allure Labs, Inc.

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.