NDC | 59886-349-66 |
Set ID | bbe4eb9d-4672-46d1-b6e5-4b6d1d737ed9 |
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
Aloe Barbadensis (Aloe Vera) Leaf Extract, Alumina,
Aluminum Stearate, Avena Satina (Oat) Kernel Oil, C20-40 Acid, Calendula
Officinalis Flower Oil, Camellia Sinensis Leaf Extract, Caprylic / Capric Triglyceride,
Cetyl Dimethicone, Cetyl PEG/PPG 10/1 Dimethicone, Chamomile Oil, Coco
Nucifera (Coconut) Oil, Cyclomethicone, Diazolidinyl Urea, Dimethicone, Ethylhexyl
Palmitate, Fragrance, Hydrogenated Castor Oil, Isododecane, Methylparaben,
Mineral Oil, Panthenol, Polyethylene, Polyhydroxystearic Acid, Propylene Glycol,
Propylparaben, Sodium Chloride, Tocopheryl Acetate, Water. - Questions or Comments?
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PRINCIPAL DISPLAY PANEL
Dr. Fischer ULTRASOL
nature BABY Sunscreen Lotion SPF50
Broad Spectrum UVA and UVB Protection
Pediatrician Recommended
With Oatmeal and Aloe Vera
SCIENCE INSIDETM SUPERIOR SUN TECHNOLOGY
VERY WATER RESISTANT
Hypoallergenic
Non-Irritating
Ophthalmologically Tested
RECOMMENDED SKIN CANCER FOUNDATION
200 ML. 6.77 FL. OZ.
FISCHER PHARMACEUTICALS
Manufactured by:
Fischer Pharmaceuticals Ltd.
Bnei Brak, Israel, 51553
Made in Israel
www.dr-fischer.com
Dr. Fischer - Tried and Tested
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INGREDIENTS AND APPEARANCE
ULTRASOL NATURE BABY SUNSCREEN
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59886-349 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP) Titanium Dioxide 15 g in 100 g Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 8 g in 100 g Inactive Ingredients Ingredient Name Strength ALUMINUM OXIDE (UNII: LMI26O6933) Aluminum Stearate (UNII: U6XF9NP8HM) Coconut Oil (UNII: Q9L0O73W7L) Methylparaben (UNII: A2I8C7HI9T) Panthenol (UNII: WV9CM0O67Z) Propylene Glycol (UNII: 6DC9Q167V3) Propylparaben (UNII: Z8IX2SC1OH) Sodium Chloride (UNII: 451W47IQ8X) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59886-349-66 200 g in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 06/10/2010 Labeler - Fischer Pharmaceuticals Ltd (600158976) Establishment Name Address ID/FEI Business Operations Fischer Pharmaceuticals Ltd 600158976 manufacture