Santi-Gel Instant Hand Sanitizer is a Topical Solution in the Human Otc Drug category. It is labeled and distributed by Kutol Products Company, Inc.. The primary component is Alcohol.
Product ID | 50865-056_6534f9bf-67e6-1c2e-e053-2a91aa0aea07 |
NDC | 50865-056 |
Product Type | Human Otc Drug |
Proprietary Name | Santi-Gel Instant Hand Sanitizer |
Generic Name | Santi-gel Instant Hand Sanitizer |
Dosage Form | Solution |
Route of Administration | TOPICAL |
Marketing Start Date | 2013-05-22 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part333A |
Labeler Name | Kutol Products Company, Inc. |
Substance Name | ALCOHOL |
Active Ingredient Strength | 63 mL/100mL |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2015-05-15 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing End Date | 2017-05-10 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-05-15 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing End Date | 2017-05-10 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing End Date | 2016-07-17 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2017-05-10 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2017-05-10 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing End Date | 2017-05-10 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing End Date | 2016-07-19 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-05-22 |
Ingredient | Strength |
---|---|
ALCOHOL | 62.5 mL/100mL |
SPL SET ID: | f5bb2593-e036-4586-a807-2049e06b2475 |
Manufacturer | |
UNII |