Arm and Hammer Orajel SensitiveFreshening with Flavor Burst (Church & Dwight Co., Inc.)
Welcome to the PulseAid listing for the Arm and Hammer Orajel Sensitive drug offered from Church & Dwight Co., 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: | Church & Dwight Co., Inc. |
NON-PROPRIETARY NAME: | Sodium Fluoride |
SUBSTANCE NAME: | SODIUM FLUORIDE; POTASSIUM NITRATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | PASTE, DENTIFRICE |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-01-29 |
END MARKETING DATE: | 0000-00-00 |
Arm and Hammer Orajel Sensitive Freshening with Flavor Burst HUMAN OTC DRUG Details:
Item Description | Arm and Hammer Orajel Sensitive Freshening with Flavor Burst from Church & Dwight Co., Inc. |
LABELER NAME: | Church & Dwight Co., Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1.1; 50(mg/g; mg/g) |
START MARKETING DATE: | 2012-01-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 10237-661_f20a5fcf-a743-4885-b573-3673e0a3def0 |
PRODUCT NDC: | 10237-661 |
APPLICATION NUMBER: | part355 |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers: