NDC | 59886-316-66 |
Set ID | 9a8a932e-c3dc-44ae-91e6-b9e3f5b21ee3 |
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,
Aminomethyl Propanol, Butylparaben, Camellia Sinensis Leaf Extract, Cetyl Dimethicone,
Chamomilla Recutita (Matricaria) Extract, Dicaprylyl Ether, Disodium EDTA, Ethylparaben,
Fragrance, Glycerin, Iodopropynyl Butylcarbamate, Isobutylparaben, Menthyl Lactate,
Methylparaben, Panthenol, Phenoxyethanol, Potassium Cetyl Phosphate, Propane / Butane /
Isobutane, Propylparaben, Sorbitane Oleate, Tocopheryl Acetate, VP/Eicosene Copolymer,
Water. - Questions or Comments?
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PRINCIPAL DISPLAY PANEL
Dr. Fischer
ULTRASOL
KIDS Sunscreen Mousse SPF30
Broad Spectrum
UVA and UVB Protection
Dermatologist Recommended
Fun Melon Fragrance
SCIENCE INSIDETM SUPERIOR SUN TECHNOLOGY
VERY WATER RESISTANT
Hypoallergenic
200 ML. 6.77 FL. OZ.
FISCHER PHARMACEUTICALS
Manufactured by:
Fischer Pharmaceuticals Ltd.
Bnei Brak, Israel, 51553
Made in Israel
www.dr-fischer.com
24m
NO CFCs
NO ANIMAL INGREDIENTS NO ANIMAL TESTING
Dr. Fischer - Tried and Tested
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INGREDIENTS AND APPEARANCE
ULTRASOLSUNSCREEN KIDS SUNSCREEN MOUSSE
avobenzone, octinoxate, octisalate, octocrylene, oxybenzone aerosol, foamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59886-316 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 Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 9 g in 100 g Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 4 g in 100 g Inactive Ingredients Ingredient Name Strength Butylparaben (UNII: 3QPI1U3FV8) EDETATE DISODIUM (UNII: 7FLD91C86K) Ethylparaben (UNII: 14255EXE39) Glycerin (UNII: PDC6A3C0OX) Methylparaben (UNII: A2I8C7HI9T) Panthenol (UNII: WV9CM0O67Z) Phenoxyethanol (UNII: HIE492ZZ3T) Propylparaben (UNII: Z8IX2SC1OH) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Propane (UNII: T75W9911L6) Butane (UNII: 6LV4FOR43R) Isobutane (UNII: BXR49TP611) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59886-316-66 200 g in 1 CAN Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 04/10/2010 Labeler - Fischer Pharmaceuticals Ltd. (600158976) Establishment Name Address ID/FEI Business Operations Fischer Pharmaceuticals Ltd. 600158976 manufacture