NDC | 59886-326-77 |
Set ID | 5d5141b0-f8e3-4fda-adfc-5d0f22d1e2b4 |
Category | HUMAN OTC DRUG LABEL |
Packager | Fischer Pharmaceuticals Ltd |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
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PRINCIPAL DISPLAY PANEL
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
- Uses
- Warnings
- Directions
- Other Information
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Inactive Ingredients
Acrylates / 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?
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INGREDIENTS AND APPEARANCE
ULTRASOLSUNSCREEN SUNSCREEN FACE CREAM SPF 34
avobenzone, octinoxate, octisalate, oxybenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59886-326 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 2 g in 100 g Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 7.5 g in 100 g Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 3 g in 100 g Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 3 g in 100 g Inactive Ingredients Ingredient Name Strength Butylparaben (UNII: 3QPI1U3FV8) Chlorphenesin (UNII: I670DAL4SZ) EDETATE DISODIUM (UNII: 7FLD91C86K) Ethylparaben (UNII: 14255EXE39) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) Isopropyl Myristate (UNII: 0RE8K4LNJS) Methylparaben (UNII: A2I8C7HI9T) Phenoxyethanol (UNII: HIE492ZZ3T) Propylene Glycol (UNII: 6DC9Q167V3) Propylparaben (UNII: Z8IX2SC1OH) Sodium Hydroxide (UNII: 55X04QC32I) Stearic Acid (UNII: 4ELV7Z65AP) Stearyl Alcohol (UNII: 2KR89I4H1Y) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59886-326-77 1 in 1 BOX 1 50 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 03/01/2010 Labeler - Fischer Pharmaceuticals Ltd (600158976) Establishment Name Address ID/FEI Business Operations Fischer Pharmaceuticals Ltd 600158976 manufacture