NDC 75990-605

Recens

Alcohol

Recens is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Certus Medical, Inc.. The primary component is Alcohol.

Product ID75990-605_1dcf9d41-b5d2-4d5d-994e-ef2f487a072a
NDC75990-605
Product TypeHuman Otc Drug
Proprietary NameRecens
Generic NameAlcohol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2019-10-16
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333E
Labeler NameCertus Medical, Inc.
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 75990-605-01

1200 mL in 1 CARTRIDGE (75990-605-01)
Marketing Start Date2020-06-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 75990-605-05 [75990060505]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-10 [75990060510]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-06 [75990060506]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16
Marketing End Date2018-11-28

NDC 75990-605-24 [75990060524]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-07 [75990060507]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-15 [75990060515]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-19
Marketing End Date2019-10-16

NDC 75990-605-14 [75990060514]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-19
Marketing End Date2019-10-16

NDC 75990-605-17 [75990060517]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16
Marketing End Date2018-11-28

NDC 75990-605-27 [75990060527]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-08 [75990060508]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-19
Marketing End Date2019-10-16

NDC 75990-605-01 [75990060501]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-28 [75990060528]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-09 [75990060509]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-19
Marketing End Date2019-10-16

NDC 75990-605-12 [75990060512]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-55 [75990060555]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16
Marketing End Date2018-11-28

NDC 75990-605-03 [75990060503]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-13 [75990060513]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

NDC 75990-605-11 [75990060511]

Recens GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-16

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:839487e4-a036-4b00-8f42-4890e4165526
Manufacturer
UNII
UPC Code
  • 0816760010162

    • NDC Crossover Matching brand name "Recens" or generic name "Alcohol"

    NDCBrand NameGeneric Name
    75990-605RecensRecens
    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 [Recens]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    RECENS
    RECENS
    88840992 not registered Live/Pending
    RecensMedical.Inc.
    2020-03-19
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