76138-122 NDC - 1902 HAND SANITIZER ()

Drug Information

  • Product NDC: 76138-122
  • Proprietary Name: 1902 HAND SANITIZER
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Innovation Specialties
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/6/2020
End Marketing Date:7/31/2023

Package Information

No. Package Code Package Description Billing Unit
176138-122-0159 mL in 1 BOTTLE (76138-122-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC76138-122The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME1902 HAND SANITIZERThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/6/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE7/31/2023The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
APPLICATION NUMBERpart333AThis is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEInnovation SpecialtiesProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

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This page was last updated on: 12/19/2025

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