LUXE COLOR FOUNDATION - Guangzhou Huixue Biotechnology Co., Ltd.

Manufacturer
Guangzhou Huixue Biotechnology Co., Ltd.
Effective date
2026-07-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-29 05:10:16

Label at a glance#

ProductLUXE COLOR FOUNDATION
Active ingredientOCTINOXATE, ZINC OXIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7% Zinc Oxide 5%

INACTIVE INGREDIENT SECTION

WATER, BUTYLENE GLYCOL,C15-19 ALKANE, DIBUTYL ADIPATE, CYCLOPENTASILOXANE,ISONONYL ISONONANOATE, BIFIDA FERMENT FILTRATE, PHENYLBENZIMIDAZOLE SULFONIC ACID, SILICA, PEG-30 DIPOLYHYDROXYSTEARATE, TRIMETHYLSILOXYSILICATE, POLYMETHYLSILSESQUIOXANE, NIACINAMIDE, GALACTOMYCES FERMENT FILTRATE, QUATERNIUM-18 BENTONITE, ISODODECANE,PHENOXYETHANOL, BISABOLOL, MAGNESIUM SULFATE, PEG-10 DIMETHICONE, POLYHYDROXYSTEARIC ACID, PORTULACA OLERACEA EXTRACT, DIMETHICONE CROSSPOLYMER, CI 77492, SODIUM HYDROXIDE, ALUMINUM HYDROXIDE, HYDRATED SILICA, TRIETHOXYCAPRYLYLSILANE, DIMETHICONE, CI 77491, SILICA DIMETHYL SILYLATE, DISTEARDIMONIUM HECTORITE, GLYCERIN, 1,2-HEXANEDIOL, TOCOPHEROL,HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, HYDROXYACETOPHENONE, HYDROXYPHENYL PROPAMIDOBENZOIC ACID, PHYLLANTHUS EMBLICA FRUIT EXTRACT, ROSA ROXBURGHII FRUIT EXTRACT, SOPHORA FLAVESCENS ROOT EXTRACT, TRIBULUS TERRESTRIS FRUIT EXTRACT, CORNUS OFFICINALIS FRUIT EXTRACT.

OTC - PURPOSE SECTION

Helps prevent sunburn. If used as directed with other sun nrntection mensures (see Directionc) decreases the risk of skin cancer and early skin aging caused by the sun.

INDICATIONS & USAGE SECTION

Helps prevent sunburn. If used as directed with other sun nrntection mensures (see Directionc) decreases the risk of skin cancer and early skin aging caused by the sun.Directions Apply liberally 15 minutes before sun exposure Reapply at least every 2 hours Use a water-resistant sunscreen if Swimming or Sweating Children under 6 months: ask c doctor

WARNINGS SECTION

For external use only Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove Stop use and ask a doctor if rash occurs Keep out of reach of children, If swallowed, get medical help or contact a Poison Control Center immediately

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Protect this product from excessive heat and direct sun Store at 15-30°℃ (59-86°F)

OTC - WHEN USING SECTION

Apply liberally 15 minutes before sun exposure Reapply at least every 2 hours Use a water-resistant sunscreen If swimming or sweating Children under 6 months ask a docton

OTC - DO NOT USE SECTION

Do not use on damaged on broken skin,Children under 6 months: ask a doctor

DOSAGE & ADMINISTRATION SECTION

Apply evenly to clean skin before sun exposure. Massage in a circular motion with your fingers until the shade blends with your skin tone. Lightweight and breathable, it offers long-lasting wear for a flawless, natural finish.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LUXE COLOR FOUNDATIONLUXE COLOR FOUNDATIONLUXE COLOR FOUNDATION

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87204-24887204-248-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LUXE COLOR FOUNDATIONOCTINOXATE 7% ZINC OXIDE 5%Guangzhou Huixue Biotechnology Co., Ltd.576c3496-702f-808c-e063-6394a90a53c32026-07-25WarningsExact identifier
ndc (package): 87204-248-01
ndc (product): 87204-248
ndc11 (package): 87204024801
spl id: 576c3496-7030-808c-e063-6394a90a53c3
spl set id: 576c3496-702f-808c-e063-6394a90a53c3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.