The Flower Uv Intense Pact
FDA Label NDC 51523-024

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Thefaceshop Co., Ltd. for the product The Flower Uv Intense Pact (NDC 51523-024). 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, description, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredients: ZINC OXIDE, TITANIUM DIOXIDE

Inactive Ingredient

Inactive Ingredients:

MICA(CI 77019), TALC, METHYL METHACRYLATE CROSSPOLYMER, ETHYLHEXYL METHOXYCINNAMATE, BORON NITRIDE, PHENYL TRIMETHICONE, DIMETHICONE, SILICA,
ETHYLHEXYL PALMITATE, IRON OXIDES(CI 77492), TRIETHOXYCAPRYLYLSILANE, METHICONE, CAPRYLIC/CAPRIC TRIGLYCERIDE, METHYLPARABEN, IRON OXIDES(CI 77491),
FRAGRANCE, IRON OXIDES(CI 77499), HYDROGENATED LECITHIN, BUTYLPARABEN, ROSA CANINA FLOWER, JASMINUM OFFICINALE (JASMINE) FLOWER,
ANTHEMIS NOBILIS FLOWER POWDER, PHALAENOPSIS AMABILIS EXTRACT, DENDROBIUM PHALAENOPSIS FLOWER EXTRACT, CAMELLIA JAPONICA FLOWER EXTRACT,
LILIUM CANDIDUM BULB EXTRACT, IMPATIENS BALSAMINA FLOWER EXTRACT, PELARGONIUM GRAVEOLENS EXTRACT, CALENDULA OFFICINALIS FLOWER EXTRACT,
HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, TROPAEOLUM MAJUS FLOWER/LEAF/STEM EXTRACT

Description

Warnings:
When using this product
Keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if
Rash or irritation develops and lasts.

Directions:
Apply evenly before sun exposure and as needed.

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