UltrasolSunscreenSunscreen Spray Lotion SPF 15 (Fischer pharmaceuticals Ltd.)
Welcome to the PulseAid listing for the UltrasolSunscreen drug offered from Fischer pharmaceuticals Ltd.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: | Fischer pharmaceuticals Ltd. |
NON-PROPRIETARY NAME: | Avobenzone, Octinoxate, Oxybenzone |
SUBSTANCE NAME: | AVOBENZONE; OCTINOXATE; OXYBENZONE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | SPRAY |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2010-03-01 |
END MARKETING DATE: | 0000-00-00 |
UltrasolSunscreen Sunscreen Spray Lotion SPF 15 HUMAN OTC DRUG Details:
Item Description | UltrasolSunscreen Sunscreen Spray Lotion SPF 15 from Fischer pharmaceuticals Ltd. |
LABELER NAME: | Fischer pharmaceuticals Ltd. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 2; 7.5; 4(g/100g; g/100g; g/100g) |
START MARKETING DATE: | 2010-03-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 59886-330_2b1ca574-2c21-4aba-8b89-0c24d34385f1 |
PRODUCT NDC: | 59886-330 |
APPLICATION NUMBER: | part352 |
Other AVOBENZONE; OCTINOXATE; OXYBENZONE Pharmaceutical Manufacturers / Labelers: