NDC 24794-138
SaniTyze
Hand Sanitizer
SaniTyze is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Crosstex International Inc.. The primary component is Alcohol.
| Product ID | 24794-138_207f332f-8be6-4803-b353-649cf8d3b40c |
| NDC | 24794-138 |
| Product Type | Human Otc Drug |
| Proprietary Name | SaniTyze |
| Generic Name | Hand Sanitizer |
| Dosage Form | Gel |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2019-01-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part333E |
| Labeler Name | Crosstex International Inc. |
| Substance Name | ALCOHOL |
| Active Ingredient Strength | 21 mL/30mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
Packaging
NDC 24794-138-04
532 mL in 1 BOTTLE (24794-138-04)
| Marketing Start Date | 2019-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 24794-138-01 [24794013801]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-06 [24794013806]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-08 [24794013808]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-07 [24794013807]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-02 [24794013802]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-03 [24794013803]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-12 [24794013812]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-05 [24794013805]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-04 [24794013804]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-10 [24794013810]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-09 [24794013809]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
NDC 24794-138-11 [24794013811]
SaniTyze GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-01-01 |
| Marketing End Date | 2020-02-02 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| ALCOHOL | 21 mL/30mL |
OpenFDA Data
| SPL SET ID: | a7ce8018-21c5-4cdb-8006-2da0d82e842d |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
NDC Crossover Matching brand name "SaniTyze" or generic name "Hand Sanitizer"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 24794-138 | SaniTyze | Hand Sanitizer |
| 24794-400 | Sanityze | ALCOHOL |
| 19355-106 | 1 Hotel Hand Sanitizer | Hand Sanitizer |
| 40303-001 | 75% Alcohol Hand Sanitizer | Hand Sanitizer |
| 40303-002 | 75% Alcohol Hand Sanitizer | Hand Sanitizer |
| 40303-003 | 75% Alcohol Hand Sanitizer | Hand Sanitizer |
| 19355-104 | Baccarat Hotel Signature Scented Hand Sanitizer | Hand Sanitizer |
| 19355-103 | Balance Hand Sanitizer | Hand Sanitizer |
| 10827-0002 | CLAIRES | HAND SANITIZER |
| 19355-102 | Energize Hand Sanitizer | Hand Sanitizer |
| 19355-113 | Five Wits Green Olive Hand Sanitizer | Hand Sanitizer |
| 23261-100 | Foaming Hand Sanitizer | Hand Sanitizer |
| 14341-006 | HAND SANITIZER | HAND SANITIZER |
| 19355-111 | Hand Sanitizer | Hand Sanitizer |
| 19355-112 | Hand Sanitizer | Hand Sanitizer |
| 35561-354 | Hand Sanitizer | Hand Sanitizer |
| 10827-0003 | ICING | HAND SANITIZER |
| 18018-501 | INSTANT HAND SANITIZER | HAND SANITIZER |
| 40303-004 | INSTANT HAND SANITIZER | HAND SANITIZER |
| 40303-005 | INSTANT HAND SANITIZER | HAND SANITIZER |
| 40303-006 | INSTANT HAND SANITIZER | HAND SANITIZER |
| 0316-0292 | Keri Clinical Care Hand Sanitizing Gel | Hand Sanitizer |
| 0316-0214 | Keri Clinical Care Hand Sanitizing Gel - HEALTHCARE | Hand Sanitizer |
| 19355-109 | PhytogenX Coronavirus Hand Sanitizer | Hand Sanitizer |
| 19355-101 | Relax Hand Sanitizer | Hand Sanitizer |
| 19355-107 | Rose Sanitizer | Hand Sanitizer |
| 37520-001 | skin care hand sanitizer | hand sanitizer |
| 37520-002 | skin care hand sanitizer | hand sanitizer |
| 19355-114 | Weaver Hand Sanitizer | Hand Sanitizer |
| 30142-803 | Winter Apple | Hand Sanitizer |
Trademark Results [SaniTyze]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SANITYZE 78719432 not registered Dead/Abandoned |
Crosstex International, Inc. 2005-09-23 |
 SANITYZE 77753025 not registered Dead/Abandoned |
Crosstex International, Inc. 2009-06-05 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.