74285-0001 NDC - BATCH 206 HAND SANITIZER ()

Drug Information

Product NDC: 74285-0001
Proprietary Name: Batch 206 Hand Sanitizer
Non Proprietary Name:
Active Ingredient(s):
Administration Route(s):
Dosage Form(s):

Labeler Information

Field Name	Field Value
Labeler Name:	Batch 206 Distillery
Product Type:
FDA Application Number:	part333A
Marketing Category:	OTC MONOGRAPH NOT FINAL
Start Marketing Date:	4/1/2020

Package Information

No.	Package Code	Package Description	Billing Unit
1	74285-0001-2	750 mL in 1 BOTTLE (74285-0001-2)
2	74285-0001-3	1892.71 mL in 1 BOTTLE (74285-0001-3)
3	74285-0001-4	3785.41 mL in 1 BOTTLE (74285-0001-4)
4	74285-0001-5	18927.1 mL in 1 JUG (74285-0001-5)
5	74285-0001-6	1022061.1817 mL in 1 CONTAINER (74285-0001-6)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	74285-0001	This is the date that the labeler indicates was the start of its marketing of the drug product.
PROPRIETARY NAME	Batch 206 Hand Sanitizer	Product 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.
START MARKETING DATE	4/1/2020	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
MARKETING CATEGORY NAME	OTC MONOGRAPH NOT FINAL	Name of Company corresponding to the labeler code segment of the Product NDC.
APPLICATION NUMBER	part333A	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
LABELER NAME	Batch 206 Distillery	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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