VivierSkin Sun Protection description, usages, side effects, indications, overdosage, supplying and lots more!

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VivierSkin Sun Protection

Vivier Pharma, Inc.

VivierSkin Sun Protection SPF45


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

4.8% Zinc Oxide
7.8% Titanium Dioxide
7.5% Parsol MCX* (Octinoxate)

Purpose

Sunscreen

VivierSkin Sun Protection Uses

Provides a sun protection factor of 45.
Provides broad spectrum UVA/UVB protection.
Ideal for daily use; can be applied under makeup.
The sun may cause sunburn, premature aging of the skin and skin cancer. Avoiding the sun, wearing protective clothing and regular use of sunscreens over the years may reduce the chance of these harmful effects.

Warnings

For external use only

When using this product

Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

Rash or irritation develops.

Keep out of reach of children

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

Directions

Apply daily to face, neck and chest.
Apply liberally and evenly 15 to 30 minutes prior to sun exposure and as needed.
Reapply as needed or after swimming, towel drying, perspiring heavily or washing.
For use on children under 6 months of age, consult a physician.

Inactive Ingredients

Water/Eau, C12-C15 Alkyl Benzoate, Alumina, Methicone, Polyhydroxystearic Acid, Triethoxy Caprylylsilane, Cyclomethicone, Dimethicone Copolyol, Cetyl Dimethicone, PEG 150, Decyl Alcohol, SMDI Copolymer, Sodium Chloride, DMDM Hydantoin, Iodopropynyl Butylcarbamate.

Questions

450 455 9779                      1 877 484 8437

Store at room temperature (15-30°C / 59-86°F).
Oil free. Alcohol-free. Fragrance-free.

Mfd. for Vivier Pharma
Hudson, QC, Canada J0P 1H0
Champlain NY 12919
Made in Canada
Prod. #80040 07-8040-10
www.vivierpharma.com

NDC 67226-2045-1















VivierSkin Sun Protection

VivierSkin Sun Protection

VivierSkin Sun Protection

ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67226-2045
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 4.8 mL
titanium dioxide 7.5 mL
OCTINOXATE OCTINOXATE 7.5 mL

Inactive Ingredients

Ingredient Name Strength
water
ALKYL (C12-15) BENZOATE
ALUMINUM OXIDE
POLYHYDROXYSTEARIC ACID (2300 MW)
TRIETHOXYCAPRYLYLSILANE
cyclomethicone
DIMETHICONE
DIMETHICONE
polyethylene glycol 6000
1-Decanol
SODIUM CHLORIDE
DMDM HYDANTOIN
IODOPROPYNYL BUTYLCARBAMATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 100 in 1 TUBE
2 60 in 1 BOTTLE, PUMP
3 NDC:67226-2045-6 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-03-25


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