NDC 61924-102
HAND-E-FOAM
Otc Antimicrobial Drug Products
HAND-E-FOAM is a Topical Aerosol, Foam in the Human Otc Drug category. It is labeled and distributed by Dermarite Industries, Llc. The primary component is Benzethonium Chloride.
Product ID | 61924-102_777faa78-a73f-1236-e053-2a91aa0ac3ec |
NDC | 61924-102 |
Product Type | Human Otc Drug |
Proprietary Name | HAND-E-FOAM |
Generic Name | Otc Antimicrobial Drug Products |
Dosage Form | Aerosol, Foam |
Route of Administration | TOPICAL |
Marketing Start Date | 2002-08-08 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part333A |
Labeler Name | DermaRite Industries, LLC |
Substance Name | BENZETHONIUM CHLORIDE |
Active Ingredient Strength | 0 g/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |