NEOGEN DERMALOGY Day-Light Protection Sun Screen SPF50 (OUTIN FUTURES CORP.)
Welcome to the PulseAid listing for the NEOGEN DERMALOGY Day-Light Protection Sun Screen SPF50 drug offered from OUTIN FUTURES CORP.. 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: | OUTIN FUTURES CORP. |
NON-PROPRIETARY NAME: | TITANIUM DIOXIDE, ZINC OXIDE, OCTINOXATE |
SUBSTANCE NAME: | TITANIUM DIOXIDE; ZINC OXIDE; OCTINOXATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2017-06-29 |
END MARKETING DATE: | 0000-00-00 |
NEOGEN DERMALOGY Day-Light Protection Sun Screen SPF50 HUMAN OTC DRUG Details:
Item Description | NEOGEN DERMALOGY Day-Light Protection Sun Screen SPF50 from OUTIN FUTURES CORP. |
LABELER NAME: | OUTIN FUTURES CORP. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | .42; 1.31; 3.51(g/46.78g; g/46.78g; g/46.78g) |
START MARKETING DATE: | 2017-06-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 69924-006_331833cc-e5bc-4340-97e9-44f9d6840f2e |
PRODUCT NDC: | 69924-006 |
APPLICATION NUMBER: | part352 |
Other TITANIUM DIOXIDE; ZINC OXIDE; OCTINOXATE Pharmaceutical Manufacturers / Labelers: