NDC 51811-375 Hand Sanitizer
NDC Product Code 51811-375
Proprietary Name: 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 51811 - Hanover Pen Corp Dba Hpc Global
- 51811-375 - Hand Sanitizer
NDC 51811-375-18
Package Description: 237 mL in 1 BOTTLE, PLASTIC
NDC 51811-375-28
Package Description: 237 mL in 1 BOTTLE, PLASTIC
NDC Product Information
Hand Sanitizer with NDC 51811-375 is a product labeled by Hanover Pen Corp Dba Hpc Global. The generic name of Hand Sanitizer is . The product's dosage form is and is administered via form.
Labeler Name: Hanover Pen Corp Dba Hpc Global
Dosage Form: -
Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
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.
- TROLAMINE (UNII: 9O3K93S3TK)
- 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 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. Values = ‘Y’ or ‘N’.
* 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
- Purpose
- Uses
- Warnings
- Do Not Use
- Stop Use And Ask A Doctor
- Keep Out Of Reach Of Children
- Directions
- Inactive Ingredients
Active Ingredient
Ethyl Alcohol 66.5%
Purpose
Antiseptic
Uses
For handwashing to decrease bacteria on skin without soap and water.Recommended for repeated use.
Warnings
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.
Directions
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.