NDC 54057-304 Alcohol Free Foam Sanitizer

NDC Product Code 54057-304

NDC 54057-304-60

Package Description: 1000 mL in 1 BAG

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Alcohol Free Foam Sanitizer with NDC 54057-304 is a product labeled by Afflink, Inc.. The generic name of Alcohol Free Foam Sanitizer is . The product's dosage form is and is administered via form.

Labeler Name: Afflink, Inc.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
  • POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
  • IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
  • D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Afflink, Inc.
Labeler Code: 54057
Start Marketing Date: 11-12-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Alcohol Free Foam Sanitizer Product Label Images

Alcohol Free Foam Sanitizer Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Alcohol Free Foam Sanitizer

​Active IngredientBenzalkonium Chloride 0.13%

  • UsesUse in a variety of public facilities.Use this product when soap and water are not available.

  • WarningsFor external use only.Avoid contact with eyes.Children under the age of 6 should be supervised by an adult when using this product.Discontinue use is irritation or redness develops.If irritation persists for more than 72 hours, consult a physician.KEEP OUT OF REACH OF CHILDREN.

  • Directions​Read the entire label before using this product.​Dispense 1-2 pumps of product onto dry hands. Rub hands together to distribute product

Inactive IngredientsDeionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, DMDM Hydantoin, PEG-3 Cocamide, Fragrance, Iodoproynyl Btylcarbamate, D&C Green #5.

PurposeAntiseptic

KEEP OUT OF REACH OF CHILDREN

AFFEX Cleaning SolutionsAlcohol Free Foam SanitizerNon Alcohol hand SanitizerMediucal Emergency:(800)424-9300NET CONTENTS: 1000 mLITEM #304-60

* Please review the disclaimer below.