Sani-Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by American Industrial Supply, Inc.. The primary component is Alcohol.
Product ID | 50519-221_60c9f9c4-032c-45a3-85db-2239d362ccc5 |
NDC | 50519-221 |
Product Type | Human Otc Drug |
Proprietary Name | Sani-Gel |
Generic Name | Alcohol |
Dosage Form | Gel |
Route of Administration | TOPICAL |
Marketing Start Date | 2009-12-01 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part333 |
Labeler Name | American Industrial Supply, Inc. |
Substance Name | ALCOHOL |
Active Ingredient Strength | 1 mL/mL |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2009-12-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part333 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-01 |
Inactivation Date | 2019-10-21 |
Ingredient | Strength |
---|---|
ALCOHOL | .7 mL/mL |
SPL SET ID: | b9d34ee8-896c-464d-b4fc-a1d844bf4b3f |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
50519-221 | Sani-Gel | Sani-Gel |
0363-0370 | Advanced Hand Sanitizer | Alcohol |
0363-9776 | Advanced Hand Sanitizer | Alcohol |
0363-0046 | Alcohol | Alcohol |
0074-9857 | Alcohol - Hand Sanitizer | Alcohol |
0065-8000 | Alcohol Antiseptic 80% | Alcohol |
0404-0122 | Antibacterial | alcohol |
0395-0040 | Ethyl Rubbing Alcohol | Alcohol |
0363-0968 | Hand Sanitizer | ALCOHOL |
0219-2020 | Humphreys Alcoholado Maravilla | ALCOHOL |
0404-5988 | Instant Hand Sanitizer | alcohol |
0295-9025 | Nozin Nasal Sanitizer | Alcohol |
0362-6000 | SeptoSan | Alcohol |
0362-6001 | SeptoSan | Alcohol |
0362-6002 | SeptoSan | Alcohol |
0064-1050 | TRISEPTIN | ALCOHOL |
0363-1305 | Walgreens | Alcohol |
0363-1306 | Walgreens | Alcohol |
0363-1307 | Walgreens | Alcohol |
0363-1308 | Walgreens | Alcohol |
0363-1309 | Walgreens | Alcohol |
0363-0969 | Walgreens Advanced Hand Sanitizer Citrus Scent | Alcohol |
0363-9005 | Walgreens Advanced Hand Sanitizer Made with Plant-Based Ethyl Alcohol | Alcohol |
0363-9003 | Walgreens Advanced Hand Sanitizer with Aloe and Vitamin E | Alcohol |
0363-0967 | WALGREENS ADVANCED HAND SANITIZER WITH FRESH SCENT | ALCOHOL |
0363-9004 | Walgreens Advanced Hand Sanitizer with Vitamin E | Alcohol |
0363-9008 | Walgreens Advanced Hand Sanitizer with Vitamin E | Alcohol |
0363-9006 | Walgreens Hand Sanitizer Coastal Breeze Scent | Alcohol |
0363-9007 | Walgreens Hand Sanitizer Crisp Apple Scent | Alcohol |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SANI-GEL 75240816 2231386 Live/Registered |
ENERGIZER BRANDS II LLC 1997-01-21 |
SANI-GEL 74302763 not registered Dead/Abandoned |
Tec Laboratories, Inc. 1992-08-10 |