NDC 75230-001
hand sanitizer
Ethyl Alcohol
hand sanitizer is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Zhejiang Hongshiliang Health Technology Co., Ltd.. The primary component is Alcohol.
| Product ID | 75230-001_a35c7cb4-4cfb-b1aa-e053-2995a90a9c27 |
| NDC | 75230-001 |
| Product Type | Human Otc Drug |
| Proprietary Name | hand sanitizer |
| Generic Name | Ethyl Alcohol |
| Dosage Form | Gel |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2020-03-21 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part333E |
| Labeler Name | Zhejiang Hongshiliang Health Technology Co., Ltd. |
| Substance Name | ALCOHOL |
| Active Ingredient Strength | 65 mL/100mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
Packaging
NDC 75230-001-01
60 BOX in 1 CARTON (75230-001-01) > 1 BOTTLE in 1 BOX > 37 mL in 1 BOTTLE
| Marketing Start Date | 2020-03-21 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 75230-001-01 [75230000101]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
NDC 75230-001-02 [75230000102]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
NDC 75230-001-09 [75230000109]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
NDC 75230-001-10 [75230000110]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
NDC 75230-001-04 [75230000104]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
NDC 75230-001-06 [75230000106]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
NDC 75230-001-05 [75230000105]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
NDC 75230-001-03 [75230000103]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
NDC 75230-001-07 [75230000107]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
NDC 75230-001-08 [75230000108]
hand sanitizer GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| ALCOHOL | 65 mL/100mL |
OpenFDA Data
| SPL SET ID: | a30d8ded-7822-8a99-e053-2995a90ab33e |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
NDC Crossover Matching brand name "hand sanitizer" or generic name "Ethyl Alcohol"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0065-9800 | HAND SANITIZER | Isopropyl Alcohol |
| 0113-7077 | hand sanitizer | ethyl alcohol |
| 0363-0469 | Hand Sanitizer | Ethyl Alcohol |
| 0363-0596 | Hand Sanitizer | Ethyl Alcohol |
| 0363-0643 | Hand Sanitizer | Ethyl Alcohol |
| 0363-0826 | Hand Sanitizer | Ethyl Alcohol |
| 0363-0890 | Hand Sanitizer | Ethyl Alcohol |
| 0363-0898 | Hand Sanitizer | Ethyl Alcohol |
| 0363-0968 | Hand Sanitizer | ALCOHOL |
| 67751-011 | HAND SANITIZER | HAND SANITIZER |
| 68016-370 | Hand Sanitizer | Hand Sanitizer |
| 68196-370 | Hand Sanitizer | Hand Sanitizer |
| 68196-951 | Hand Sanitizer | Hand Sanitizer |
| 0519-8802 | Hand Sanitizer | Hand Sanitizer |
| 69092-001 | Hand Sanitizer | Hand Sanitizer |
| 69674-100 | Hand Sanitizer | Hand Sanitizer |
| 69790-770 | Hand Sanitizer | Hand Sanitizer |
| 69831-0001 | Hand Sanitizer | Hand Sanitizer |
| 69842-784 | Hand Sanitizer | Hand Sanitizer |
| 69947-120 | Hand Sanitizer | Hand Sanitizer |
| 70000-0462 | Hand Sanitizer | Hand Sanitizer |
| 70000-0320 | Hand Sanitizer | Hand Sanitizer |
| 70124-110 | Hand Sanitizer | Hand Sanitizer |
| 70675-958 | HAND SANITIZER | HAND SANITIZER |
| 71011-001 | HAND SANITIZER | HAND SANITIZER |
| 71063-001 | Hand Sanitizer | Hand Sanitizer |
| 71089-002 | Hand Sanitizer | Hand Sanitizer |
| 71087-001 | Hand Sanitizer | Hand Sanitizer |
| 71087-002 | Hand Sanitizer | Hand Sanitizer |
| 71154-001 | Hand Sanitizer | Hand Sanitizer |
| 71011-003 | HAND SANITIZER | HAND SANITIZER |
| 70939-002 | Hand sanitizer | Hand sanitizer |
| 70939-001 | Hand sanitizer | Hand sanitizer |
| 71011-005 | HAND SANITIZER | HAND SANITIZER |
| 71141-153 | Hand Sanitizer | Hand Sanitizer |
| 71569-370 | Hand Sanitizer | Hand Sanitizer |
| 71828-001 | Hand Sanitizer | Hand Sanitizer |
| 71927-005 | Hand Sanitizer | Hand Sanitizer |
| 72131-005 | Hand Sanitizer | Hand Sanitizer |
| 71927-004 | Hand Sanitizer | Hand Sanitizer |
| 72036-370 | Hand Sanitizer | Hand Sanitizer |
| 72131-001 | Hand Sanitizer | Hand Sanitizer |
| 71927-001 | Hand Sanitizer | Hand Sanitizer |
| 72131-004 | Hand Sanitizer | Hand Sanitizer |
| 72024-770 | Hand Sanitizer | Hand Sanitizer |
| 72264-003 | Hand Sanitizer | Hand Sanitizer |
| 71927-002 | Hand Sanitizer | Hand Sanitizer |
| 72264-002 | Hand Sanitizer | Hand Sanitizer |
| 72131-003 | Hand Sanitizer | Hand Sanitizer |
| 72180-001 | Hand Sanitizer | Hand Sanitizer |
Trademark Results [hand sanitizer]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HAND SANITIZER 88958909 not registered Live/Pending |
MAISON BLANCHE, LLC 2020-06-10 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.