Epionce Ultra Shield description, usages, side effects, indications, overdosage, supplying and lots more!

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Epionce Ultra Shield

Episciences, Inc.
Episciences, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Purpose

Sunscreen

Warnings

For external use only

Do not use

on damaged or broken skin

Stop use

and ask a doctor if rash occurs

When using this product

keep out of eyes.
Rinse with water to remove.

Keep out of reach of children.

If product is swallowed, get medical help or contact
a Poison Control Center right away.

Ask a doctor

children under 6 months

Questions?

Call toll free 1-800-374-6623

Inactive Ingredients

Water, Alkyl (C12-15) Benzoate, Caprylyl Trisiloxane,
Butylene Glycol, Glycerin, Hydrogenated Polybutene
(1300 MW), Meadowfoam Seed Oil, Steareth-21, Dimethicone,
Trimethylsiloxysilicate (M/Q 0.66), Ammonium
Acryloyldimethyltaurate/VP Copolymer, Caprylyl
Glycol, Safflower Oil, Cetostearyl Alcohol, Ethylhexylglycerin,
Hexylene Glycol, Hydroxyethyl Acrylate/Sodium
Acryloyldimethyl Taurate Copolymer (45000 MPA.S AT
1%), Linseed Oil, Malic Acid, Phenoxyethanol, Date,
Polyhydroxystearic Acid (2300 MW), Polysorbate 80,
Steareth-2, Triethoxycaprylylsilane.

Directions

helps prevent sunburn

• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours
• Sun Protection Measures. Spending time in the
sun increases your risk of skin cancer and early skin
aging. To 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-sleeved shirts, pants, hats and sunglasses

Other Information

• protect this product from excessive heat and direct sun

Active Ingredients

Zinc Oxide 10.1%
Homosalate 10.0%
Octisalate 5.0%

Drug Facts

Epionce Ultra Shield

Epionce Ultra Shield

Zinc Oxide, Homosalate, Octisalate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42673-001
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 0.101 mL
HOMOSALATE Homosalate 0.10 mL
OCTISALATE OCTISALATE 0.05 mL

Inactive Ingredients

Ingredient Name Strength
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
BUTYLENE GLYCOL
ALKYL (C12-15) BENZOATE
CAPRYLYL GLYCOL
CAPRYLYL TRISILOXANE
SAFFLOWER OIL
CETOSTEARYL ALCOHOL
DIMETHICONE
ETHYLHEXYLGLYCERIN
GLYCERIN
Hexylene Glycol
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)
MEADOWFOAM SEED OIL
LINSEED OIL
Malic Acid
PHENOXYETHANOL
DATE
POLYHYDROXYSTEARIC ACID (2300 MW)
polysorbate 80
STEARETH-2
TRIETHOXYCAPRYLYLSILANE
water
TRIMETHYLSILOXYSILICATE (M/Q 0.66)

Product Characteristics

Color
white

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42673-001-01 75 in 1 TUBE
2 NDC:42673-001-03 6 in 1 TUBE
3 NDC:42673-001-04 453 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-04-06


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