ANTIMICROBIAL FOAMING SANITIZER is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by A-cute Derm, Incorporated. The primary component is Benzethonium Chloride.
| Product ID | 61619-718_228d0fc2-16c8-2b16-e054-00144ff88e88 |
| NDC | 61619-718 |
| Product Type | Human Otc Drug |
| Proprietary Name | ANTIMICROBIAL FOAMING SANITIZER |
| Generic Name | Benzethonium Chloride Liquid |
| Dosage Form | Liquid |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2015-10-27 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part333A |
| Labeler Name | A-Cute Derm, Incorporated |
| Substance Name | BENZETHONIUM CHLORIDE |
| Active Ingredient Strength | 0 g/100g |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2015-10-27 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-10-27 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-10-27 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-10-27 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| BENZETHONIUM CHLORIDE | .2 g/100g |
| SPL SET ID: | 228e3c11-613e-5535-e054-00144ff88e88 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 37945-718 | ANTIMICROBIAL FOAMING SANITIZER | Benzethonium chloride liquid |
| 61619-718 | ANTIMICROBIAL FOAMING SANITIZER | Benzethonium chloride liquid |
| 37945-902 | ANTIMICROBIAL FACE BODY WASH | Benzethonium chloride liquid |