High Five is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Jani-source, Llc. The primary component is Alcohol.
Product ID | 49557-221_1a602bf9-674c-4705-bb9b-91f6dd1b6b4a |
NDC | 49557-221 |
Product Type | Human Otc Drug |
Proprietary Name | High Five |
Generic Name | Alcohol |
Dosage Form | Gel |
Route of Administration | TOPICAL |
Marketing Start Date | 2013-08-01 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part333E |
Labeler Name | Jani-Source, LLC |
Substance Name | ALCOHOL |
Active Ingredient Strength | 1 mL/mL |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2013-08-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-01 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
ALCOHOL | .7 mL/mL |
SPL SET ID: | 72c9bb48-e947-45fd-a2aa-e16a3af7f9f7 |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
49557-221 | High Five | High Five |
49557-575 | High Five | High Five |
49557-572 | High Five | High Five |
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