Dosage Administration Section
DOSAGE ADMINISTRATION SECTION
Lumibronze Mineral Spf 30 Bronzing Face Serum Liquid
FDA Label NDC 87593-108
7 label sections · Submitted to the FDA by Lance (guangzhou) Biological Technology Co., Ltd. · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lance (guangzhou) Biological Technology Co., Ltd. for the product Lumibronze Mineral Spf 30 Bronzing Face Serum (NDC 87593-108). 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 section, inactive ingredient section, indications usage section, keep out of reach of children section, purpose section, warnings section, lumibronze mineral spf 30 bronzing face serum, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient Section
INACTIVE INGREDIENT SECTION
Indications Usage Section
INDICATIONS USAGE SECTION
Keep Out Of Reach Of Children Section
KEEP OUT OF REACH OF CHILDREN SECTION
Purpose Section
PURPOSE SECTION
Warnings Section
WARNINGS SECTION
Lumibronze Mineral Spf 30 Bronzing Face Serum
LumiBronze Mineral SPF 30 Bronzing Face Serum
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