Dosage & Administration
Apply to the face or body.
Sunscreen
FDA Label NDC 84025-034
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Yanxi Biotechnology Co., Ltd for the product Sunscreen (NDC 84025-034). 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 dosage & administration, inactive ingredient, otc - keep out of reach of children, warnings, otc - purpose, indications & usage, 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
Inactive Ingredient
aqua
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Warnings
For external use only.
Otc - Purpose
helps prevent sunburn
Indications & Usage
Apply liberally 15 minutes before sun exposure. Reapply: After 80 minutes of swimming or sweating, Immediately after towel drying, At least every 2 hours.
Package Label.Principal Display Panel
84025-034 (0c618b327c0f2fae3e0e8f99a8b1d0a)
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