ActivOn Ultra Strength Arthritis (Family First Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the ActivOn Ultra Strength Arthritis drug offered from Family First Pharmaceuticals, 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: | Family First Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | Menthol and Histamine Dihydrochloride |
| SUBSTANCE NAME: | MENTHOL, UNSPECIFIED FORM; HISTAMINE DIHYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | STICK |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2011-09-01 |
| END MARKETING DATE: | 0000-00-00 |
ActivOn Ultra Strength Arthritis HUMAN OTC DRUG Details:
| Item Description | ActivOn Ultra Strength Arthritis from Family First Pharmaceuticals, Inc. |
| LABELER NAME: | Family First Pharmaceuticals, Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | .04574; .00028(g/g; g/g) |
| START MARKETING DATE: | 2011-09-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51068-501_6a97a677-5c25-4d3a-9593-3191f6a981bd |
| PRODUCT NDC: | 51068-501 |
| APPLICATION NUMBER: | part348 |
Other MENTHOL, UNSPECIFIED FORM; HISTAMINE DIHYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
