SurfersSkin Sunscreen Zinc description, usages, side effects, indications, overdosage, supplying and lots more!

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SurfersSkin Sunscreen Zinc

Skin Alive, Ltd.

SurfersSkin Sunscreen Zinc




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients

Octinoxate 7.5%

Titanium Dioxide 2.35%

Zinc Oxide 4.2%

Purpose

Purpose

Sunscreen

Uses

Uses

Helps prevent sunburn

Higher SPF gives more sunburn protection

Provides high protection against sunburn

Regains SPF after 80 minutes of sweating.

Warnings

For external use only

UV exposure from the sun increases the risk of skin cancer, premature skin aging and other skin damage. It is important to decrease UV exposure by limiting time in the sun, wearing protective clothing and using a sunscreen.


When using this product

Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

if irritation occurs or rash develops and lasts.

Directions

apply generously 15mins before sun exposure and as needed

Children under 6 months of age: ask a doctor.

Reapply as needed or after towel drying, swimming or sweating.

Inactive Ingredients

Butylated Hydroxytoluene, Castor oil, Fragrance, Hydrogenated castor oil, Iron Oxides, Kaolin, Oleyl-alcohol, paraffin wax, petroleum jelly, sunflower oil, Talc

SurfersSkin SPF 30+ Sunscreen Zinc gives great protection especially in the snow. Apply liberally to face, nose and lips.


To report a serious adverse event, contact 1-800-332-1088

Expires:

Lot Number:

ww.snowskin.co

DIST. BY Quiver Dist, Bend Oregon, USA 97701

Tested on Snowboarders - Not animals

AS/ANZ STANDARD 2604-1998

Net Wt. 0.30oz (8.5g)

SPF 30+

very water / sweat resistant

broad spectrum

UVA/UVB protection



Proven in extreme new zealand conditions

SufersSkin sunscreen Zinc

hands free

Net Wt. 0.30oz (8.5g)

contains no nanoparticles-aminobenzoic acid (PABA) free

SurfersSkin Sunscreen Zinc

SurfersSkin Sunscreen Zinc

SurfersSkin Sunscreen Zinc

OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE STICK

Product Information

Product Type Human otc drug label Item Code (Source) NDC:75916-0636
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 7.5 g
titanium dioxide 2.35 g
Zinc Oxide Zinc oxide 4.2 g

Inactive Ingredients

Ingredient Name Strength
BUTYLATED HYDROXYTOLUENE
castor oil
HYDROGENATED CASTOR OIL
IRON
KAOLIN
OLEYL ALCOHOL
PARAFFIN
petrolatum
SUNFLOWER OIL
talc

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 8.5 in 1 TUBE, WITH APPLICATOR
2 NDC:75916-0636-1 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-01-27


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