FDA Label for Quiksilver Spf 30 Sunscreen 01
View Indications, Usage & Precautions
Quiksilver Spf 30 Sunscreen 01 Product Label
The following document was submitted to the FDA by the labeler of this product Shenzhen Lantern Scicence Co.,ltd.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Drug Facts
Active Ingredient
Active Ingredient Purpose
Avobenzone 1.0%
Ethylhexyl Methoxycinnamate 8.0%
Homosalate 2.0%
Octocrylene 2.0% ..........................................Sunscreen
Inactive Ingredients
AQUA,CYCLOPENTASILOXANE,ISOHEXADECANE,ETHYLHEXYL METHOXYCINNAMATE,GLYCERIN,BUTYLENE GLYCOL,CETYL PEG/PPG-10/1 DIMETHICONE,HOMOSALATE,OCTOCRYLENE,SODIUM CHLORIDE,AVOBENZONE,POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE,DISTEARDIMONIUM HECTORITE,PHENOXYETHANOL,HYDROXYACETOPHENONE,PARFUM,BISABOLOL,DISODIUM EDTA.
Directions
Apply liberaaly 15 minutes before sun exposure.
Children under 6 months; Ask a doctor.
Otc - Do Not Use
When using this product
keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Do not inhale or ingest.
Avoid contact with broken skin.
Other Information
Do not store above 105F.
May discolor some fabrics.
Harmful to wood finishes and plastics.
Protect the product in this container from excessive heat and direct sun.
For sunscreen use
Apply to all skin exposed to the sun
Limit time in the sun,especially from 10 a.m.-2 p.m.
Wear long-s;eeved shirts,pants,hats,and sunglasses.
When Using This Product
Keep out of eyes,Rinse with water to remove.
Purpose
Sunscreen
Stop Use And Ask A Doctor
if rash occurs.
Do Not Use
on danaged or broken skin.
Package Label.Principal Display Panel
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