NDC 75990-007

Celox Ultra

Alcohol

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

Product ID75990-007_87ae6fae-62b6-42f3-9e18-394f2c039677
NDC75990-007
Product TypeHuman Otc Drug
Proprietary NameCelox Ultra
Generic NameAlcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2011-04-25
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333E
Labeler NameCertus Medical, Inc.
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 75990-007-16

236 mL in 1 BOTTLE, PLASTIC (75990-007-16)
Marketing Start Date2011-04-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 75990-007-03 [75990000703]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-08 [75990000708]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-05 [75990000705]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-17 [75990000717]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-27 [75990000727]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-28 [75990000728]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-12 [75990000712]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-24 [75990000724]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-09 [75990000709]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-10 [75990000710]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-01 [75990000701]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-14 [75990000714]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-16 [75990000716]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-18 [75990000718]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-07 [75990000707]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-30 [75990000730]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-06 [75990000706]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-15 [75990000715]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-13 [75990000713]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-11 [75990000711]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

NDC 75990-007-55 [75990000755]

Celox Ultra LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-25
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:15b2d102-3c18-4b1d-bfa9-4575af4c9e00
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 582753

    • NDC Crossover Matching brand name "Celox Ultra" or generic name "Alcohol"

    NDCBrand NameGeneric Name
    75990-007Celox UltraCelox Ultra
    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
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