DISINFECTION HAND SANITIZER GEl is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Huizhou Baozi Biotechnology Co., Ltd.. The primary component is Alcohol.
Product ID | 74881-001_a2c35647-40f3-5ef5-e053-2a95a90a9da0 |
NDC | 74881-001 |
Product Type | Human Otc Drug |
Proprietary Name | DISINFECTION HAND SANITIZER GEl |
Generic Name | Disinfection Hand Sanitizer Gel |
Dosage Form | Gel |
Route of Administration | TOPICAL |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part333A |
Labeler Name | Huizhou Baozi Biotechnology Co., Ltd. |
Substance Name | ALCOHOL |
Active Ingredient Strength | 75 mL/100mL |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2020-04-08 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-08 |
Ingredient | Strength |
---|---|
ALCOHOL | 75 mL/100mL |
SPL SET ID: | a2c35647-40f5-5ef5-e053-2a95a90a9da0 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |