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Dr Marvel COLOR CHANGING FOUNDATION SPF30 drug information

ETHYLHEXYL METHOXYCINNAMATE
Guangzhou Liyan Cosmetics Technology Co., Ltd. · TOPICAL

Product NDC: 87770-013

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Generic nameETHYLHEXYL METHOXYCINNAMATE
Labeler / manufacturerGuangzhou Liyan Cosmetics Technology Co., Ltd.
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC87770-013
Label effective date2026-08-24

Official product label reference

Dr Marvel COLOR CHANGING FOUNDATION SPF30 — Guangzhou Liyan Cosmetics Technology Co., Ltd.

This page contains 7 source sections for ETHYLHEXYL METHOXYCINNAMATE, topical route. Label set 59c8865f-ccee-dd50-e063-6294a90aa185, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Indications & Usage • Helps prevent sunburn. • If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun.

Purpose

Evens out skin texture, conceals dullness, brightens complexion, gently protects against UV rays, and creates a natural, seamless base.
Dosage and administration — label text
Directions • Adults and children 6 months of age and older: Apply generously and evenly 15 minutes before sun exposure. • Reapply at least every 2 hours. • Children under 6 months of age: Ask a doctor.
Warnings
Warnings • Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product helps prevent sunburn; it does not reduce the risk of skin cancer or early skin aging. • For external use only. • Do not use on broken or damaged skin. • Avoid contact with eyes. If contact occurs, rinse thoroughly with water. • Stop use and consult a doctor if skin rash develops. • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Inactive ingredient
AQUA BUTYLENE GLYCOL CI 77891 ISOHEXADECANE C12-15 ALKYL BENZOATE CETYL PEG/PPG-10/1 DIMETHICONE GLYCERIN TRIMETHYLSILOXYSILICATE MICA DIMETHICONE CYCLOPENTASILOXANE SODIUM CHLORIDE PANTHENOL DIISOSTEARYL MALATE MAGNESIUM STEARATE PHENOXYETHANOL DISTEARDIMONIUM HECTORITE CI 77492 DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER TRIETHOXYCAPRYLYLSILANE SQUALANE CI 77491 ALUMINUM HYDROXIDE ETHYLHEXYLGLYCERIN CI 77499 POLYVINYL ALCOHOL 1,2-HEXANEDIOL TREMELLA FUCIFORMIS (MUSHROOM) EXTRACT SODIUM POLYACRYLATE OPUNTIA DILLENII EXTRECT AVENA SATIVA (OAT) EXTRACT BHT FUCUS VESICULOSUS EXTRACT ASTRAGALUS MEMBRANACEUS EXTRACT SCUTELLARIA BAICALENSIS ROOT EXTRACT ATRACTYLODES MACROCEPHALA ROOT EXTRACT SAPOSHNIKOVIA DIVARICATA ROOT EXTRACT HIBISCUS ABELMOSCHUS EXTRACT GLYCYRRHIZA INFLATA EXTRACT CENTELLA ASIATICA EXTRACT
Child safety
Warnings • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Recent major changes
Directions • Adults and children 6 months of age and older: Apply generously and evenly 15 minutes before sun exposure. • Reapply at least every 2 hours. • Children under 6 months of age: Ask a doctor.

Official sources and product identifiers

Substances listed: ETHYLHEXYL SALICYLATE, OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE

Package NDC codes

87770-013-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.