Skin Crave non-alcohol Hand Sanitizer is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Tropical Enterprises International, Inc.. The primary component is Benzalkonium Chloride.
| Product ID | 58418-786_48440f5b-7f26-224a-e054-00144ff8d46c |
| NDC | 58418-786 |
| Product Type | Human Otc Drug |
| Proprietary Name | Skin Crave non-alcohol Hand Sanitizer |
| Generic Name | Antibacterial Non-alcohol Hand Sanitizer |
| Dosage Form | Spray |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2012-08-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part333A |
| Labeler Name | Tropical Enterprises International, Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Active Ingredient Strength | 13 mg/mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2012-08-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| BENZALKONIUM CHLORIDE | 13 mg/mL |
| SPL SET ID: | 2bb0c814-13e7-35c7-e054-00144ff8d46c |
| Manufacturer | |
| UNII |