NDC 68878-118 Theochem Foaming Hand Sanitizer

NDC Product Code 68878-118

NDC CODE: 68878-118

Proprietary Name: Theochem Foaming Hand Sanitizer What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 68878 - Theochem Laboratories Inc

NDC 68878-118-10

Package Description: 1250 mL in 1 BOTTLE, DISPENSING

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

NDC Product Information

Theochem Foaming Hand Sanitizer with NDC 68878-118 is a product labeled by Theochem Laboratories Inc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1038799.

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)

Product Labeler Information

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

Labeler Name: Theochem Laboratories Inc
Labeler Code: 68878
Start Marketing Date: 10-01-2008 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: 12-31-2017 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.

Theochem Foaming Hand Sanitizer Product Label Images

Theochem Foaming Hand 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

Active Ingredient

Benzalkonium Chloride 0.1%




- For hand sanitizing to decrease bacteria on the skin.- Recommended for repeated use.


For external use only.When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.


- Pump a small amount of foam into palm of hand.- Rub throughly over all surfaces of both hands.- Rub hands together briskly until dry.

Other Information

Store below 110 °F (43 °C). May discolor certain fabrics or surfaces.

Inactive Ingredients

Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereteh-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide.

* Please review the disclaimer below.