Otc - Active Ingredient
Active Ingredients: Ethylhexyl Methoxycinnamate, Zinc Oxide, 4-Methylbenzylidene camphor, Butyl Mehoxydibenzoylmethane
Medispa Sunblock
FDA Label NDC 52554-1001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Universal Cosmetic Co., Ltd for the product Medispa Sunblock (NDC 52554-1001). 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, description, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Description
Uses■ Perfectly blocks both UVA and UVB rays without stimuli■ Provides high protection from sunburn■ Suitable for skin that underwent medical treatmentWarningFor external use onlyWhen using this product■ Avoid eye area. If contact occurs, rinse eyes thoroughly■ Discontinue use if signs of irritation developsKeep out of reach of the childrenDirection■ Rub a proper quantity over the whole face, before finishing skincare.Other Information■ store between 20-25 °C (68-77 °F)■ avoid freezing and excessive heat above 40 °C (104 °F)■ close cap after use.Inactive Ingredient■ Water ■ Cyclomethicone ■ Dimethicone/Vinyl Dimethicone Crosspolymer ■ C12-15 Alkyl Benzoate ■ Glycerin ■ Cetyl PEG/PPG-10/1 Dimethicone ■ Beeswax ■ Sodium Chloride ■ Sorbitan Sesquiolate ■ C20-40 acid ■ Methylparaben ■ Polyethylene ■ Brassica Campestris Sterols ■ Propylparaben ■ Disodium EDTA
* Please review the disclaimer below.
