Putto Secret Uv Face
FDA Label NDC 75885-040

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Agabang & Company for the product Putto Secret Uv Face (NDC 75885-040). 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, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

titanium dioxide


Inactive Ingredient

houttuynia cordata ext, glechoma hederacea flower/leaf/stem ext, plantago asiatica ext, cyclopentasiloxane, butylene glycol, crprylic/capric triglyceride, dipropylene glycol, morus alba leaf ext, ulmus davidiana root ext, zinc oxide, squalane, peg-10 dimethicone, cetyl peg/ppg-10/1 dimethicone, sodium chloride, dimethicone/vinyl dimethicone crosspolymer, dimethicone, stearalkonium hectorite, propylene carbonate, aluminum hydroxide, peg-9 polydimethylsiloxyethyl dimethicone, stearic acid,hydrogen dimethicone, caprylhydroxamic acid, caprylyl glycol, glycerin, 1,2-hexanediol, tocopheryl acetate betaine, panthenol, ceramide 3, distearyldimonium chloride, sodium hyaluronate, beta-glucan, bentonite, fragrance

Otc - Purpose

sun screen


Otc - Keep Out Of Reach Of Children

keep out of reach of the children


Indications & Usage

gently spread a fair amount over face, neck, arm and etc esposed to UV rays


Warnings

do not apply to sensitive skin
store in a cool, dry place


Dosage & Administration

for external use only


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