UltrasolSunscreen Sunscreen Face Cream SPF 34

Dosage form: cream
Ingredients: Avobenzone 2g in 100g, Octinoxate 7.5g in 100g, Octisalate 3g in 100g, Oxybenzone 3g in 100g
Labeler: Fischer Pharmaceuticals Ltd
NDC Code: 59886-326

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Dr. Fischer ULTRASOL Sunscreen Face Cream SPF34


 


Dr. Fischer ULTRASOL

Sunscreen Face Cream SPF34

Broad Spectrum UVA and UVB Protection

Dermatologist Recommended

SCIENCE INSIDETM SUPERIOR SUN TECHNOLOGY

VERY WATER RESISTANT

Hypoallergenic

Sensitive approved

50 ML. 1.69 FL. OZ.

RECOMMENDED - SKIN CANCER FOUNDATION

Manufactured by:

Fischer Pharmaceuticals Ltd.

Bnei Brak, Israel, 51553

Made in Israel

www.dr-fischer.com

24m

NO ANIMAL TESTING - NO ANIMAL INGREDIENTS

Extra moisture for delicate face and neck areas

Moisturizing Care and Sun Protection

Light Texture

Rapidly Absorbed

Soothes and calms the skin with Chamomile

Vitamin E and Green Tea antioxidant protection against free radicals

Tested according to the most stringent international sunscreen standards

This product is recommended by the American Skin Cancer Foundation as an effective UV sunscreen

FISCHER PHARMACEUTICALS

Dr. Fischer - Tried and Tested


Drug Facts

Active Ingredients                                                                             Purpose
Avobenzone 2.0%, Octinoxate 7.5%, Octisalate 3.0%,
Oxybenzone 3.0% ........................................................................ Sunscreen

Uses

• helps prevent sunburn • higher SPF gives more sunburn
protection • helps protect the skin against the harmful effects of UVA and
UVB rays • retains SPF after 80 minutes of activity in the water or
sweating

Warnings

For external use only

When using this product

avoid contact with the eyes. If contact occurs
rinse thoroughly with water.

Stop use and ask a doctor if

rash or irritation develops and lasts.

Keep out of reach of children.

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

Directions

• apply generously and evenly to all exposed areas before
sun exposure • reapply as needed or after towel drying, swimming,
perspiring or vigorous activity • children under 6 months of age: ask a
doctor

Other Information

• may stain some fabrics • Sun alert: Limiting
sun exposure, wearing protective clothing, and using sunscreens may
reduce the risks of skin aging, skin cancer, and other harmful effects of
the sun.

Inactive IngredientsAcrylates / C10-30 Alkyl Acrylate Crosspolymer,
Butylparaben, Chlorophenesin, Disodium EDTA, Ethylparaben,
Fragrance, Glyceryl Stearate, Green Tea (Camellia Sinensis) Leaf Extract,
Iodopropynyl Butylcarbamate, Isopropyl Myristate, Methylparaben,
Phenoxyethanol, Polyethylene, Potassium Cetyl Phosphate, Propylene Glycol,
Propylparaben, Sodium Hydroxide, Stearic Acid, Stearyl Alcohol, Tocopheryl
Acetate, Water.

Questions or Comments?

Call 1-877-212-1985 Mon-Fri

ULTRASOLSUNSCREEN  SUNSCREEN FACE CREAM SPF 34
avobenzone, octinoxate, octisalate, oxybenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59886-326
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (Avobenzone) Avobenzone2 g  in 100 g
Octinoxate (Octinoxate) Octinoxate7.5 g  in 100 g
Octisalate (Octisalate) Octisalate3 g  in 100 g
Oxybenzone (Oxybenzone) Oxybenzone3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Butylparaben 
Chlorphenesin 
EDETATE DISODIUM 
Ethylparaben 
GLYCERYL MONOSTEARATE 
Isopropyl Myristate 
Methylparaben 
Phenoxyethanol 
Propylene Glycol 
Propylparaben 
Sodium Hydroxide 
Stearic Acid 
Stearyl Alcohol 
ALPHA-TOCOPHEROL ACETATE 
Water 
Packaging
#Item CodePackage Description
1NDC:59886-326-771 TUBE (TUBE) in 1 BOX
150 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/01/2010
Labeler - Fischer Pharmaceuticals Ltd (600158976)
Establishment
NameAddressID/FEIOperations
Fischer Pharmaceuticals Ltd600158976manufacture

Revised: 02/2010
 
Fischer Pharmaceuticals Ltd

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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