Otc - Active Ingredient
Octinoxate
Sunscreen Cream
FDA Label NDC 87243-123
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Maidora Co.,ltd for the product Sunscreen (NDC 87243-123). 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, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive 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 - Purpose
helps prevent sunburn
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Indications & Usage
helps prevent sunburn
apply liberally 15 minutes before sun exposure
after 80 minutes of swimming or sweating
immediately after towel drying
Warnings
keep out of eyes. Rinse with water to remove
Dosage & Administration
helps prevent sunburn
Inactive Ingredient
Water,Propylene Glycol,Dimethicone,Sodium Dilauramidoglutamide Lysine,Tocopheryl Acetate,Butylene Glycol,Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Carbomer,Ceteareth-10,Sodium Hydroxide,BHT,Methylparaben
Package Label.Principal Display Panel
1 (1)
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