HUSKY 515 Instant Hand Sanitizer is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Canberra Corporation. The primary component is Alcohol.
Product ID | 63779-515_0206e7a2-15db-4d8c-bccf-f4e096b791cb |
NDC | 63779-515 |
Product Type | Human Otc Drug |
Proprietary Name | HUSKY 515 Instant Hand Sanitizer |
Generic Name | Ethanol |
Dosage Form | Gel |
Route of Administration | TOPICAL |
Marketing Start Date | 1998-10-28 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part333E |
Labeler Name | Canberra Corporation |
Substance Name | ALCOHOL |
Active Ingredient Strength | 600 mL/L |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 1998-10-28 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1998-10-28 |
Inactivation Date | 2019-11-13 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1998-10-28 |
Inactivation Date | 2019-11-13 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1998-10-28 |
Inactivation Date | 2019-11-13 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-02-16 |
Inactivation Date | 2019-11-13 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1998-10-28 |
Inactivation Date | 2019-11-13 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1998-10-28 |
Inactivation Date | 2019-11-13 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1998-10-28 |
Inactivation Date | 2019-11-13 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1998-10-28 |
Inactivation Date | 2019-11-13 |
Ingredient | Strength |
---|---|
ALCOHOL | 600 mL/L |
SPL SET ID: | fb80370d-9bf8-4cb0-9bff-d8b7ccd4ee07 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
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