NDC 51811-375 Hand Sanitizer

NDC Product Code 51811-375

NDC 51811-375-18

Package Description: 237 mL in 1 BOTTLE, PLASTIC

NDC 51811-375-28

Package Description: 237 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Hand Sanitizer with NDC 51811-375 is a product labeled by Hanover Pen Corp Dba Hpc Global. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:

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.

  • ALOE (UNII: V5VD430YW9)
  • 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: Hanover Pen Corp Dba Hpc Global
Labeler Code: 51811
Start Marketing Date: 02-01-2012 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: 12-31-2018 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.

Hand Sanitizer Product Label Images

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

Ethyl Alcohol 66.5%




For handwashing to decrease bacteria on skin without soap and water.Recommended for repeated use.


For external use only.Flammable, keep away from fire or flame.

Do Not Use

Do not use in the eyes. If this happens rinse throughly with water

Stop Use And Ask A Doctor

Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours.

Keep Out Of Reach Of Children

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


Wet hands throughly with productallow to dry without wiping   children under six should be supervised while using this produce.

Inactive Ingredients

Aloe vera, carbomer, fragrance, purified water, triethanolamine

* Please review the disclaimer below.