NDC 78082-026 Alcohol Wipes 75% Alcohol

Honour Hand Sanitizing Wipes 75% Alcohol

NDC Product Code 78082-026

NDC 78082-026-01

Package Description: 300 CLOTH in 1 BAG

NDC 78082-026-02

Package Description: 800 CLOTH in 1 BAG

NDC 78082-026-03

Package Description: 150 CLOTH in 1 BAG

NDC Product Information

Alcohol Wipes 75% Alcohol with NDC 78082-026 is a a human over the counter drug product labeled by Pico Inc.. The generic name of Alcohol Wipes 75% Alcohol is honour hand sanitizing wipes 75% alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Pico 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.

Alcohol 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/1001

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: Pico Inc.
Labeler Code: 78082
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: 05-18-2021 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 - NO 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 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

Main Ingredients

75% alcohol



Indications & Usage

Open the lid and the sticker, pull out the wipes needed and then press the sticker back and close the lid to avoid alcohol evaporation.


Contains 75% ethanol alcohol. Keep away from heat and fire source. Place in dry and cool areas

Otc - Do Not Use

Do not use on sensitive position, like face eye, nose and mouth

Otc - When Using

1. Contains 75% ethanol alcohol. Keep away from heat and fire source. Place in dry and cool areas

2. Keep away from Children

3. Do not use on sensitive position, like face eye, nose and mouth

4. Do not flush into toilet

Otc - Stop Use


Otc - Keep Out Of Reach Of Children

Keep away from Children

Dosage & Administration


Storage And Handling


Inactive Ingredients

Purified water (aqua), Aloe Leaf Extract, Glycerin, Benzalkonium chloride

Package 800 Wipes

800 wipes NDC 78082-026-02

Package 150 Wipes

150 Wipes NDC 78082-026-03

* Please review the disclaimer below.