Garnier Ombrelle Kids Mineral 50 Plus Water Resistant 80 Minutes

Manufacturer
L'OREAL USA PRODUCTS INC | L'OREAL USA, INC
Effective date
2024-01-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:16:19

Label at a glance#

ProductGarnier Ombrelle Kids Mineral 50 Plus Water Resistant 80 Minutes
Active ingredientTITANIUM DIOXIDE
Label structure5 sections

Dosage and administration

Adults and children over 6 months and up. Apply generously and evenly 15 minutes before sun exposure. Reapply at least every 2 hours, after 80 minutes of swimming or sweating and immediately after towel drying.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium dioxide 15%

Warnings

WARNINGS SECTION

For external use only. When using this product avoid contact with eyes. If contact occurs, rinse thoroughlly with water. Do not use on broken skin. 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 right away. 

Directions 

DOSAGE & ADMINISTRATION SECTION

Adults and children over 6 months and up. Apply generously and evenly 15 minutes before sun exposure. Reapply at least every 2 hours, after 80 minutes of swimming or sweating and immediately after towel drying.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, dimethicone, c12-15 alkyl benzoate, isohexadecane, talc, styrene/acrylates copolymer, isododecane, caprylyl methicone, dicaprylyl ether, triethylhexanoin, dicaprylyl carbonate, dimethicone/PEG-10/15 crosspolymer, aluminum hydroxide, stearic acid, pentylene glycol, PEG-9 polydimethylsiloxyethyl dimethicone, aluminum stearate, PEG-8 laurate, phenoxyethanol, magnesium sulfate, caprylyl glycol, alumina, polyhydroxystearic acid, disteardimonium hectorite, tocopherol, propylene carbonate, PEG-9

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-87249967-872-01

Ingredients#

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

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Source Document#

Source XML

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ee3c6c6d-e6d2-4ace-9de6-90c65d5570b7ea59057e-4a1c-4985-a49f-4c483b0976792024-02-01WarningsExact identifier
spl set id: ea59057e-4a1c-4985-a49f-4c483b097679

Reported adverse events (FAERS/openFDA)#

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