NDC 75186-006
Skinact
Alcohol
Skinact is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Huizhou Duomei Daily Necessites Co.,ltd. The primary component is Alcohol.
| Product ID | 75186-006_a7598785-19d7-72bc-e053-2a95a90ab74f |
| NDC | 75186-006 |
| Product Type | Human Otc Drug |
| Proprietary Name | Skinact |
| Generic Name | Alcohol |
| Dosage Form | Gel |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2020-03-30 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part333A |
| Labeler Name | Huizhou Duomei Daily Necessites Co.,Ltd |
| Substance Name | ALCOHOL |
| Active Ingredient Strength | 75 mL/100mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
Packaging
NDC 75186-006-01
10 mL in 1 BOTTLE (75186-006-01)
| Marketing Start Date | 2020-03-30 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 75186-006-14 [75186000614]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-33 [75186000633]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-21 [75186000621]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-34 [75186000634]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-18 [75186000618]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-16 [75186000616]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-04 [75186000604]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-05 [75186000605]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-07 [75186000607]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-37 [75186000637]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-29 [75186000629]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-27 [75186000627]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-20 [75186000620]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-42 [75186000642]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-32 [75186000632]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-24 [75186000624]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-01 [75186000601]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-02 [75186000602]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-03 [75186000603]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-08 [75186000608]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-17 [75186000617]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-41 [75186000641]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-25 [75186000625]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-39 [75186000639]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-11 [75186000611]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-22 [75186000622]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-40 [75186000640]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-12 [75186000612]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-35 [75186000635]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-31 [75186000631]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-23 [75186000623]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-09 [75186000609]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-10 [75186000610]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-36 [75186000636]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-30 [75186000630]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-26 [75186000626]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-13 [75186000613]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-06 [75186000606]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-19 [75186000619]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-15 [75186000615]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-28 [75186000628]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
NDC 75186-006-38 [75186000638]
Skinact GEL
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-03-30 |
Drug Details
NDC Crossover Matching brand name "Skinact" or generic name "Alcohol"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 75186-006 | Skinact | Skinact |
| 78160-002 | Skinact | Skinact |
| 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 |
Trademark Results [Skinact]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SKINACT 87818445 5584947 Live/Registered |
SkinAct 2018-03-02 |
 SKINACT 86579666 4850517 Live/Registered |
SkinAct 2015-03-27 |
 SKINACT 77137183 3347755 Dead/Cancelled |
Hartoonians, Dro 2007-03-21 |
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