Daily Facial Moisturizer SPF 35 (Pharmco Laboratories Inc.)
Welcome to the PulseAid listing for the Daily Facial Moisturizer SPF 35 drug offered from Pharmco Laboratories Inc.. 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: | Pharmco Laboratories Inc. |
NON-PROPRIETARY NAME: | Octinoxate and Avobenzone |
SUBSTANCE NAME: | OCTINOXATE; AVOBENZONE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-06-01 |
END MARKETING DATE: | 0000-00-00 |
Daily Facial Moisturizer SPF 35 HUMAN OTC DRUG Details:
Item Description | Daily Facial Moisturizer SPF 35 from Pharmco Laboratories Inc. |
LABELER NAME: | Pharmco Laboratories Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 40; 25(mg/g; mg/g) |
START MARKETING DATE: | 2012-06-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 58400-007_f94aff8f-dae4-4b59-a519-12706799e4cd |
PRODUCT NDC: | 58400-007 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; AVOBENZONE Pharmaceutical Manufacturers / Labelers: