NDC 79519-022 Loveit-janitex Disinfecting Wipes 75% Alcohol

Ethyl Alcohol

NDC Product Code 79519-022

NDC CODE: 79519-022

Proprietary Name: Loveit-janitex Disinfecting Wipes 75% Alcohol 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: Ethyl Alcohol 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

  • 79519 - Pacific Health Systems Inc.
    • 79519-022 - Loveit-janitex Disinfecting Wipes 75% Alcohol

NDC 79519-022-01

Package Description: 80 PACKAGE in 1 CONTAINER > 4.16 mL in 1 PACKAGE

NDC Product Information

Loveit-janitex Disinfecting Wipes 75% Alcohol with NDC 79519-022 is a a human over the counter drug product labeled by Pacific Health Systems Inc.. The generic name of Loveit-janitex Disinfecting Wipes 75% Alcohol is ethyl alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Pacific Health Systems Inc.

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

Product Type: Human Otc Drug 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.

Loveit-janitex Disinfecting Wipes 75% Alcohol Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 75 mL/100mL

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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Pacific Health Systems Inc.
Labeler Code: 79519
FDA Application Number: part333A What is the FDA Application Number?
This 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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product 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.

Start Marketing Date: 02-09-2021 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: 12-31-2022 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: N 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.

Loveit-janitex Disinfecting Wipes 75% Alcohol Product Label Images

Loveit-janitex Disinfecting Wipes 75% Alcohol 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 75%




• To decrease bacteria on the skin that could cause disease.


• For external use only, harmful if swallowed.• Do not use as baby wipe.• Do not flush.• Do not use on open skin wounds.• Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.


• No need to rinse after usage. Allow skin to dry without wiping. For adults and children 2 years and over. Discard properly after use. Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

• Store in dry and cool place and away from oxidizers.• Production date, expiry date and lot number are written on the package.

Inactive Ingredients

Water (Aqua, Eau), Glycerin, Parfum

* Please review the disclaimer below.