NDC | 59886-320-55 |
Set ID | 876d12b1-51b7-409e-b43f-89583bf60709 |
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
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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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PRINCIPAL DISPLAY PANEL
Dr. Fischer Ultrasol
Sunscreen Lotion
SPF 34
Broad Spectrum
UVA and UVB Protection
Dermatologist Recommended
SCIENCE INSIDETM - SUPERIOR SUN TECHNOLOGY
VERY WATER RESISTANT
Hypoallergenic
Sensitive Approved
RECOMMENDED - SKIN CANCER FOUNDATION
250 ML. 8.45 FL.OZ.
FISCHER PHARMACEUTICALS
(Back of Package):
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
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INGREDIENTS AND APPEARANCE
ULTRASOLSUNSCREEN SUNSCREEN LOTION SPF 34
avobenzone , octinoxate, octisalate, oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59886-320 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:59886-320-55 250 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 03/01/2010 Labeler - Fischer Pharmaceuticals Ltd (600158976) Establishment Name Address ID/FEI Business Operations Fischer Pharmaceuticals Ltd 600158976 manufacture