NDC | 59886-354-55 |
Set ID | 53080a26-b800-4dcd-9479-c07df3c9c307 |
Category | HUMAN OTC DRUG LABEL |
Packager | Fischer Pharmaceuticals Ltd |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Drug Facts
- Uses
- Warnings
- Directions
- Other Information
-
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?
-
PRINCIPAL DISPLAY PANEL
Dr. Fischer
ULTRASOL
Sunscreen Lotion SPF45
Broad UVA and UVB protection
Dermatologist Recommended
SCIENCE INSIDETM SUPERIOR SUN TECHNOLOGY
VERY WATER RESISTANT
VERY SWEAT RESISTANT
NON GREASY
250 ML. 8.45 FL. OZ.
RECOMMENDED - SKIN CANCER FOUNDATION
FISCHER PHARMACEUTICALS
Manufactured by:
Fischer Pharmaceuticals Ltd.
Bnei Brak, Israel, 51553
Made in Israel
www.dr-fischer.com
NO ANIMAL INGREDIENTS - NO ANIMAL TESTING
24M
Dr. Fischer - Tried and Tested
-
INGREDIENTS AND APPEARANCE
ULTRASOL SPORT
avobenzone, octinoxate, octisalate, oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59886-354 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 5 g in 100 g Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 4 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:59886-354-55 250 g in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 06/25/2010 Labeler - Fischer Pharmaceuticals Ltd (600158976) Establishment Name Address ID/FEI Business Operations Fischer Pharmaceuticals Ltd 600158976 manufacture