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 ID75186-006_a7598785-19d7-72bc-e053-2a95a90ab74f
NDC75186-006
Product TypeHuman Otc Drug
Proprietary NameSkinact
Generic NameAlcohol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-03-30
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameHuizhou Duomei Daily Necessites Co.,Ltd
Substance NameALCOHOL
Active Ingredient Strength75 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 75186-006-01

10 mL in 1 BOTTLE (75186-006-01)
Marketing Start Date2020-03-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 75186-006-14 [75186000614]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-33 [75186000633]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-21 [75186000621]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-34 [75186000634]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-18 [75186000618]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-16 [75186000616]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-04 [75186000604]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-05 [75186000605]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-07 [75186000607]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-37 [75186000637]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-29 [75186000629]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-27 [75186000627]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-20 [75186000620]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-42 [75186000642]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-32 [75186000632]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-24 [75186000624]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-01 [75186000601]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-02 [75186000602]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-03 [75186000603]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-08 [75186000608]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-17 [75186000617]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-41 [75186000641]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-25 [75186000625]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-39 [75186000639]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-11 [75186000611]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-22 [75186000622]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-40 [75186000640]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-12 [75186000612]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-35 [75186000635]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-31 [75186000631]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-23 [75186000623]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-09 [75186000609]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-10 [75186000610]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-36 [75186000636]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-30 [75186000630]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-26 [75186000626]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-13 [75186000613]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-06 [75186000606]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-19 [75186000619]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-15 [75186000615]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-28 [75186000628]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 75186-006-38 [75186000638]

Skinact GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

Drug Details

NDC Crossover Matching brand name "Skinact" or generic name "Alcohol"

NDCBrand NameGeneric Name
75186-006SkinactSkinact
78160-002SkinactSkinact
0363-0370Advanced Hand SanitizerAlcohol
0363-9776Advanced Hand SanitizerAlcohol
0363-0046AlcoholAlcohol
0074-9857Alcohol - Hand SanitizerAlcohol
0065-8000Alcohol Antiseptic 80%Alcohol
0404-0122Antibacterialalcohol
0395-0040Ethyl Rubbing AlcoholAlcohol
0363-0968Hand SanitizerALCOHOL
0219-2020Humphreys Alcoholado MaravillaALCOHOL
0404-5988Instant Hand Sanitizeralcohol
0295-9025Nozin Nasal SanitizerAlcohol
0362-6000SeptoSanAlcohol
0362-6001SeptoSanAlcohol
0362-6002SeptoSanAlcohol
0064-1050TRISEPTINALCOHOL
0363-1305WalgreensAlcohol
0363-1306WalgreensAlcohol
0363-1307WalgreensAlcohol
0363-1308WalgreensAlcohol
0363-1309WalgreensAlcohol
0363-0969Walgreens Advanced Hand Sanitizer Citrus ScentAlcohol
0363-9005Walgreens Advanced Hand Sanitizer Made with Plant-Based Ethyl AlcoholAlcohol
0363-9003Walgreens Advanced Hand Sanitizer with Aloe and Vitamin EAlcohol
0363-0967WALGREENS ADVANCED HAND SANITIZER WITH FRESH SCENTALCOHOL
0363-9004Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
0363-9008Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
0363-9006Walgreens Hand Sanitizer Coastal Breeze ScentAlcohol
0363-9007Walgreens Hand Sanitizer Crisp Apple ScentAlcohol

Trademark Results [Skinact]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SKINACT
SKINACT
87818445 5584947 Live/Registered
SkinAct
2018-03-02
SKINACT
SKINACT
86579666 4850517 Live/Registered
SkinAct
2015-03-27
SKINACT
SKINACT
77137183 3347755 Dead/Cancelled
Hartoonians, Dro
2007-03-21

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