NDC 74238-001

CDC 70i

Isopropyl Alcohol

CDC 70i is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Friendo Llc. The primary component is Isopropyl Alcohol.

Product ID74238-001_a47053ea-6d2e-4dc3-e053-2995a90a7d42
NDC74238-001
Product TypeHuman Otc Drug
Proprietary NameCDC 70i
Generic NameIsopropyl Alcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2020-03-31
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameFriendo LLC
Substance NameISOPROPYL ALCOHOL
Active Ingredient Strength1 L/L
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 74238-001-09

.059 L in 1 BOTTLE, PLASTIC (74238-001-09)
Marketing Start Date2020-03-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 74238-001-15 [74238000115]

CDC 70i LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31

NDC 74238-001-14 [74238000114]

CDC 70i LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31

NDC 74238-001-12 [74238000112]

CDC 70i LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31

NDC 74238-001-13 [74238000113]

CDC 70i LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31

NDC 74238-001-09 [74238000109]

CDC 70i LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31

NDC 74238-001-11 [74238000111]

CDC 70i LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31

NDC 74238-001-10 [74238000110]

CDC 70i LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31

Drug Details

Active Ingredients

IngredientStrength
ISOPROPYL ALCOHOL.754 L/L

OpenFDA Data

SPL SET ID:a470a2d6-4ff1-f213-e053-2995a90a0446
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1039900

    • NDC Crossover Matching brand name "CDC 70i" or generic name "Isopropyl Alcohol"

    NDCBrand NameGeneric Name
    74238-001CDC 70iCDC 70i
    74238-101CDC 70iCDC 70i
    0363-081070%Isopropyl alcohol
    0363-084570% RubbingIsopropyl Alcohol
    0395-9103Ear Drops for SwimmersIsopropyl Alcohol
    0065-9800HAND SANITIZERIsopropyl Alcohol
    0395-1211HUMCO 1 Percent IodineIsopropyl Alcohol
    0395-0098HUMCO Ear Drops for SwimmersIsopropyl Alcohol
    0395-1249HUMCO Isopropyl Rubbing Alcohol 70%Isopropyl Alcohol
    0395-4202HUMCO Isopropyl Rubbing Alcohol 70% Professional PackIsopropyl Alcohol
    0168-0907Isopropyl AlcoholIsopropyl Alcohol
    0363-0275Isopropyl alcoholIsopropyl alcohol
    0363-0277Isopropyl alcoholIsopropyl alcohol
    0363-0472Isopropyl alcoholIsopropyl alcohol
    0363-0804Isopropyl AlcoholIsopropyl Alcohol
    0395-1260Isopropyl Alcohol Antiseptic 75% Topical SolutionIsopropyl Alcohol
    0363-0809Walgreen AlcoholIsopropyl Alcohol
    0363-6505Walgreens 70% Isopropyl Alcohol WipesISOPROPYL ALCOHOL

    Trademark Results [CDC 70i]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    CDC 70I
    CDC 70I
    88888055 not registered Live/Pending
    Friendo LLC
    2020-04-26
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