77319-0001 NDC - ULTIMATE HAND SANITIZER ()

Drug Information

  • Product NDC: 77319-0001
  • Proprietary Name: Ultimate Hand Sanitizer
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Saman
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
177319-0001-1355 mL in 1 BOTTLE (77319-0001-1)
277319-0001-2472 mL in 1 BOTTLE (77319-0001-2)
377319-0001-3800 mL in 1 BOTTLE (77319-0001-3)
477319-0001-4946 mL in 1 BOTTLE (77319-0001-4)
577319-0001-53780 mL in 1 BOTTLE (77319-0001-5)

NDC Record

Field Name Field Value Definition
PRODUCT NDC77319-0001Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEUltimate 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 DATE3/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct 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.
APPLICATION NUMBERpart333AThis is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESamanProduct 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