Sun Block
FDA Label NDC 51414-200

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Yuyao Jessie Promotional Products Co., Ltd. for the product Sun Block (NDC 51414-200). 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 active ingredient, use, warnings, direction, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

OctylMethoxycinnamate,Benzophenone-3,Homosalate, Titanium dioxide

Use

Protection from the sun’s damaging effects

Warnings

For external use only                                                         Not recommended for children under 6 months of age

Direction

Apply liberally and evenly before sun exposure.

Inactive Ingredient

Water,CetearylAlcohol,Glycerinmonostearate,                               Gctt,Propylparaben,Methylparaben,                                    glycerol,EDTA-2NA,Vinylchloride-methylacrylate,                   copolymer,Methylisothiazolinone

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