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Mineral sunscreen drug information

MINERAL SUNSCREEN
Guangzhou Origin Beauty Cosmetics Co., Ltd. · CUTANEOUS

Product NDC: 87545-002

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameMINERAL SUNSCREEN
Labeler / manufacturerGuangzhou Origin Beauty Cosmetics Co., Ltd.
RouteCUTANEOUS
Drug classDrug class not supplied in source label
Product NDC87545-002
Label effective date2026-08-19

Official product label reference

Mineral sunscreen — Guangzhou Origin Beauty Cosmetics Co., Ltd.

This page contains 10 source sections for MINERAL SUNSCREEN, cutaneous route. Label set 59713657-a7ef-1aee-e063-6394a90a326e, 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

Helps prevent sunburn. If usedas directed with other sunprotection measures (seeDirections), decreases the riskof skin cancer and early skinaging caused by the sun, Uses SECTION

Purpose

Helps prevent sunburn. If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun, Uses section
Dosage and administration — label text
Apply liberally 15 minutes before sun exposure Reapply: After 40 minutes of swimming or sweating ■Immediately after towel drying ■At least every 2 hours
Warnings
For external use only Do not use on damaged or broken skin. When using the 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 Poison Control Center right away.
Active ingredient
ZINC OXIDE [NON-NANO] ZINC OXIDE [NON-NANO]
Ask a doctor before use
Childrenunder 6 months: Ask a doctor.
Do not use
Do not use on damaged or broken skin
Child safety
Warning section Keep out of reach of children.
When to stop use and seek help
Warning section
Inactive ingredient
AcetylPeptides, Allantoin, AmmoniumAcryloyldimethyltaurate/VpCopolymer, Bisabolol, CopperTripeptide-1, Cetearyl Alcohol,Disodium Edta, Ethylhexylglyc-erin, Glycerin, Hydrolyzed Sodium Hyaluronate (Low Mw),Hydroxyacetophenone,Hydroxyethyl Acrylate/SodiumAcryloyldimethyl TaurateCopolymer, Inulin LaurylCarbamate, IsononylIsononanoate, Niacinamide,Polysorbate 60, 1,2-Hexanediol,Sodium Methyl StearoylTaurate, Sodium Hyaluronate(High Mw), SorbitanIsostearate, Squalane (Olive-Derived), Tocopheryl Acetate, Vp/Hexadecene Copolymer, Water, Xanthan Gum

Official sources and product identifiers

Substances listed: ZINC OXIDE

Package NDC codes

87545-002-01

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.