49351-016 NDC - TORK PREMIUM HAND SANITIZER FOAM ALCOHOL-FREE ()

Drug Information

  • Product NDC: 49351-016
  • Proprietary Name: Tork Premium Hand Sanitizer Foam Alcohol-Free
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: SCA Tissue North America
Product Type:
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/3/2010

Package Information

No. Package Code Package Description Billing Unit
149351-016-011 BAG in 1 BOX (49351-016-01) / 800 mL in 1 BAG
249351-016-024 BAG in 1 CARTON (49351-016-02) / 1100 mL in 1 BAG

NDC Record

Field Name Field Value Definition
PRODUCT NDC49351-016The 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 NAMETork Premium Hand Sanitizer Foam Alcohol-FreeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/3/2010This 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 NUMBERpart333This 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.
LABELER NAMESCA Tissue North AmericaName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/4/2025

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