Otc - Active Ingredient
Active ingredients: Ethylhexyl methoxycinnamate, 4-methylbenzylidene camphor, butyl methoxydibenzoylmethane, titanium dioxide, zinc oxide
Conju Princess Uv Sun Block
FDA Label NDC 59915-2001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Conju Inc for the product Conju Princess Uv Sun Block (NDC 59915-2001). 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.
Label Section Quick Index
Inactive Ingredient
Inactive ingredient: water, cyclopentasiloxane, dipropylene glycol, glycerin, dimethicone, hexyl laurate, sorbitan olivate, sorbitan sesquioleate, magnesium sulfate, stearic acid, hectorite, aluminum hydroxide, phenoxyethanol, propylparaben, methylparaben, disodium EDTA, fragrance
Otc - Purpose
Recommended for sensitive skin that needs virtually total sunblock protection
Otc - Keep Out Of Reach Of Children
Keep out of reach of the children
Indications & Usage
Apply daily, with or without make-up to exposed areas
Warnings
Avoid eye area. If contact occurs, rinse eyes thoroughly with water.If following abnormal symptoms (red specks, swelling, itching) occurs after use, stop use and ask doctor.
Dosage & Administration
Apply daily, with or without make-up to exposed areas
* Please review the disclaimer below.
