Sunblock
FDA Label NDC 52625-101

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Vienna Health And Beauty Corporation for the product Sunblock (NDC 52625-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredients:                        PurposeTitanium Dioxide 8%                        SunscreenOctyl Methoxycinnamate 6%         SunscreenOther Ingredients: Purified Water (Acqua), Capryic/Capic Triglyceride, C12-15 Alkyl Benzoate, Glycerin, Cetyl Alcohol, Stearyl Alcohol, Isopropyl Myristate, Propylene Glycol, Ceteareth-6,Ceteareth-25, Dimethocone, Glyceryl Stearate, Stearic Acid, Tocopherol Acetate(Vitamin E), Alpha Bisabolol, Triethanolamine, Diazolidinyl Urea, Methylparaben, Propylparaben, Allantoin, BHT.

Package Label.Principal Display Panel

Vienna Health and Beauty - by Minh Le, M.D. SUNBLOCK - UVA/UVB Protection - SPF30

Image Of Carton For Tub (Cartontube)

Image Of Carton For Tub (Cartontube)

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