78581-001 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 78581-001

Proprietary Name: Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: TJC Sanitizer Products LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/2020

Package Information

No. Package Code Package Description Billing Unit
178581-001-011 g in 1 BOTTLE (78581-001-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC78581-001The translation of the dosage form Code submitted by the firm.
PROPRIETARY NAMEHand 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 DATE5/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETJC Sanitizer Products LLCProduct 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: 2/1/2023