NDC 73976-1330

Santotizer

Hand Santizer Solution

Santotizer is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Santolubes Llc. The primary component is Alcohol.

Product ID73976-1330_a18cef50-abe0-a416-e053-2a95a90a83de
NDC73976-1330
Product TypeHuman Otc Drug
Proprietary NameSantotizer
Generic NameHand Santizer Solution
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2020-03-30
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameSantolubes LLC
Substance NameALCOHOL
Active Ingredient Strength80 L/100L
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 73976-1330-1

3.6 L in 1 PAIL (73976-1330-1)
Marketing Start Date2020-03-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 73976-1330-1 [73976133001]

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

NDC 73976-1330-2 [73976133002]

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

NDC 73976-1330-3 [73976133003]

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

NDC 73976-1330-4 [73976133004]

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

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL80 L/100L

OpenFDA Data

SPL SET ID:a18cef50-abdf-a416-e053-2a95a90a83de
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1039339

  • Trademark Results [Santotizer]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    SANTOTIZER
    SANTOTIZER
    88943737 not registered Live/Pending
    Vantage Santolubes Research LLC
    2020-06-02

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