NDC 74238-101

CDC 70i

Isopropyl Alcohol

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

Product ID74238-101_a22c9710-bf52-6f5f-e053-2a95a90a8ccf
NDC74238-101
Product TypeHuman Otc Drug
Proprietary NameCDC 70i
Generic NameIsopropyl Alcohol
Dosage FormGel
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 Strength3 L/4L
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 74238-101-04

4 L in 1 BOTTLE, PLASTIC (74238-101-04)
Marketing Start Date2020-03-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 74238-101-03 [74238010103]

CDC 70i GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31
Marketing End Date2020-04-27

NDC 74238-101-02 [74238010102]

CDC 70i GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31
Marketing End Date2020-04-27

NDC 74238-101-08 [74238010108]

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

NDC 74238-101-07 [74238010107]

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

NDC 74238-101-04 [74238010104]

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

NDC 74238-101-06 [74238010106]

CDC 70i GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31
Marketing End Date2020-04-28

NDC 74238-101-05 [74238010105]

CDC 70i GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-31
Marketing End Date2020-04-27

Drug Details

Active Ingredients

IngredientStrength
ISOPROPYL ALCOHOL2.8 L/4L

OpenFDA Data

SPL SET ID:a2cdcc3d-2159-de30-e053-2a95a90a0a9f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 581698

    • 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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