Sheer Tint description, usages, side effects, indications, overdosage, supplying and lots more!

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Sheer Tint

Dermalogica, Inc.

Sheer Tint SPF20


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredients

Octinoxate 4.5%,
Zinc Oxide 9.5%

Purpose

Sunscreen

Sheer Tint Uses

  • helps prevent sunburn.
  • if used as directed with other sun protection measures (see Directions), helps decrease the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only

Do not use on damaged or broken skin

When using this 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 a Poison Control Center right away.

Directions

  • apply liberally 15 minutes before sun exposure
  • reapply:
    • at least every two hours
    • use a water resistant sunscreen if swimming or sweating
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To help decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
    • limit time in the sun, especially from 10 a.m. – 2 p.m.
    • wear long-sleeve shirts, pants, hats and sunglasses
  • Children under 6 months: ask a doctor

Inactive ingredients

Water/Aqua, Caprylic/Capric Triglyceride, Butylene Glycol, Dimethicone, Methyl Gluceth-20, Lactamide MEA, Glyceryl Stearate, Stearic Acid, Cetearyl Alcohol, Sorbitan Stearate, Sorbityl Laurate, Hydrolyzed Pearl, Silanetriol, Juglans Regia (Walnut) Seed Extract, Olea Europaea (Olive) Fruit Extract, Lavandula Spica (Lavender) Flower Oil, Lavandula Hybrida Oil, Eucalyptus Globulus Leaf Oil, Lavandula Angustifolia (Lavender) Extract, Allantoin, Sodium Hyaluronate Crosspolymer, Pentylene Glycol, Glycerin, Sodium Lactate, Lactic Acid, Serine, Urea, Sorbitol, Sodium Chloride, Polysorbate 60, Cetyl Alcohol, Panthenol, Magnesium Aluminum Silicate, Xanthan Gum, Potassium Sorbate, Sodium Benzoate, Citric Acid, Disodium EDTA, Polyhydroxystearic Acid, Triethoxycaprylylsilane, Caprylhydroxamic Acid, Ethylhexylglycerin, Methylpropanediol, Silica, Iron Oxides CI 77491, CI 77492, CI 77499, Titanium Dioxide CI 77891.

Sheer Tint Other information

  • Protect this product from excessive heat and direct sun

Questions?

1-800-831-5150 in USA

PRINCIPAL DISPLAY PANEL - 40 mL Tube Carton - Light

sheer
tint

spf
20

broad
spectrum

light

1.3 US Fl. Oz.
40 mL e

dermalogica ®

Sheer Tint

PRINCIPAL DISPLAY PANEL - 40 mL Tube Carton - Medium

sheer
tint

spf
20

broad
spectrum

medium

1.3 US Fl. Oz.
40 mL e

dermalogica ®

Sheer Tint

PRINCIPAL DISPLAY PANEL - 40 mL Tube Carton - Dark

sheer
tint

spf
20

broad
spectrum

dark

1.3 US Fl. Oz.
40 mL e

dermalogica ®

Sheer Tint

Sheer Tint

Zinc Oxide and Octinoxate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68479-200
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 95 mg
OCTINOXATE OCTINOXATE 45 mg

Inactive Ingredients

Ingredient Name Strength
water
POTASSIUM SORBATE
SODIUM BENZOATE
MEDIUM-CHAIN TRIGLYCERIDES
BUTYLENE GLYCOL
methyl gluceth-20
DIMETHICONE
N-Lactoyl Ethanolamine
GLYCERYL MONOSTEARATE
STEARIC ACID
CETOSTEARYL ALCOHOL
SORBITAN MONOSTEARATE
Sorbityl Laurate
CALCIUM CARBONATE
SILANETRIOL
ENGLISH WALNUT
BLACK OLIVE
LAVENDER OIL
LAVANDIN OIL
EUCALYPTUS OIL
LAVANDULA ANGUSTIFOLIA FLOWERING TOP
ALLANTOIN
PEG-9 Diglycidyl Ether/Sodium Hyaluronate Crosspolymer
PENTYLENE GLYCOL
GLYCERIN
sodium lactate
LACTIC ACID
SERINE
UREA
sorbitol
SODIUM CHLORIDE
POLYSORBATE 60
CETYL ALCOHOL
PANTHENOL
magnesium aluminum silicate
XANTHAN GUM
CITRIC ACID MONOHYDRATE
EDETATE DISODIUM
POLYHYDROXYSTEARIC ACID (2300 MW)
TRIETHOXYCAPRYLYLSILANE
CAPRYLHYDROXAMIC ACID
ETHYLHEXYLGLYCERIN
methylpropanediol
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
titanium dioxide

Product Characteristics

Color
BROWN (Skin Tone Light)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 40 in 1 TUBE
2 NDC:68479-200-00 2 in 1 POUCH

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-09-01


Sheer Tint

Zinc Oxide and Octinoxate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68479-900
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 95 mg
OCTINOXATE OCTINOXATE 45 mg

Inactive Ingredients

Ingredient Name Strength
water
POTASSIUM SORBATE
SODIUM BENZOATE
MEDIUM-CHAIN TRIGLYCERIDES
BUTYLENE GLYCOL
methyl gluceth-20
DIMETHICONE
N-Lactoyl Ethanolamine
GLYCERYL MONOSTEARATE
STEARIC ACID
CETOSTEARYL ALCOHOL
SORBITAN MONOSTEARATE
Sorbityl Laurate
CALCIUM CARBONATE
SILANETRIOL
ENGLISH WALNUT
BLACK OLIVE
LAVENDER OIL
LAVANDIN OIL
EUCALYPTUS OIL
LAVANDULA ANGUSTIFOLIA FLOWERING TOP
ALLANTOIN
PEG-9 Diglycidyl Ether/Sodium Hyaluronate Crosspolymer
PENTYLENE GLYCOL
GLYCERIN
sodium lactate
LACTIC ACID
SERINE
UREA
sorbitol
SODIUM CHLORIDE
POLYSORBATE 60
CETYL ALCOHOL
PANTHENOL
magnesium aluminum silicate
XANTHAN GUM
CITRIC ACID MONOHYDRATE
EDETATE DISODIUM
POLYHYDROXYSTEARIC ACID (2300 MW)
TRIETHOXYCAPRYLYLSILANE
CAPRYLHYDROXAMIC ACID
ETHYLHEXYLGLYCERIN
methylpropanediol
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
titanium dioxide

Product Characteristics

Color
BROWN (Skin Tone Medium)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 40 in 1 TUBE
2 NDC:68479-900-00 118 in 1 BOTTLE, PLASTIC
3 NDC:68479-900-04 2 in 1 POUCH

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-09-01


Sheer Tint

Zinc Oxide and Octinoxate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68479-300
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 95 mg
OCTINOXATE OCTINOXATE 45 mg

Inactive Ingredients

Ingredient Name Strength
water
POTASSIUM SORBATE
SODIUM BENZOATE
MEDIUM-CHAIN TRIGLYCERIDES
BUTYLENE GLYCOL
methyl gluceth-20
DIMETHICONE
N-Lactoyl Ethanolamine
GLYCERYL MONOSTEARATE
STEARIC ACID
CETOSTEARYL ALCOHOL
SORBITAN MONOSTEARATE
Sorbityl Laurate
CALCIUM CARBONATE
SILANETRIOL
ENGLISH WALNUT
BLACK OLIVE
LAVENDER OIL
LAVANDIN OIL
EUCALYPTUS OIL
LAVANDULA ANGUSTIFOLIA FLOWERING TOP
ALLANTOIN
PEG-9 Diglycidyl Ether/Sodium Hyaluronate Crosspolymer
PENTYLENE GLYCOL
GLYCERIN
sodium lactate
LACTIC ACID
SERINE
UREA
sorbitol
SODIUM CHLORIDE
POLYSORBATE 60
CETYL ALCOHOL
PANTHENOL
magnesium aluminum silicate
XANTHAN GUM
CITRIC ACID MONOHYDRATE
EDETATE DISODIUM
POLYHYDROXYSTEARIC ACID (2300 MW)
TRIETHOXYCAPRYLYLSILANE
CAPRYLHYDROXAMIC ACID
ETHYLHEXYLGLYCERIN
methylpropanediol
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
titanium dioxide

Product Characteristics

Color
BROWN (Skin Tone Dark)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 40 in 1 TUBE
2 NDC:68479-300-00 2 in 1 POUCH

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-09-01


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Be sure to consult your doctor before taking any medication!
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