NDC 78922-001 75% Alcohol Wipes

75% Alcohol Wipes

NDC Product Code 78922-001

NDC 78922-001-01

Package Description: 50 CLOTH in 1 BAG

NDC 78922-001-02

Package Description: 80 CLOTH in 1 BAG

NDC 78922-001-03

Package Description: 100 CLOTH in 1 BAG

NDC 78922-001-04

Package Description: 100 CLOTH in 1 PAIL

NDC Product Information

75% Alcohol Wipes with NDC 78922-001 is a a human over the counter drug product labeled by Henan Meishiyu Sanitary Products Co., Ltd.. The generic name of 75% Alcohol Wipes is 75% alcohol wipes. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Henan Meishiyu Sanitary Products Co., Ltd.

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.

75% Alcohol Wipes 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/1

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.
  • 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: Henan Meishiyu Sanitary Products Co., Ltd.
Labeler Code: 78922
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: 08-26-2020 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: 12-31-2021 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.

75% Alcohol Wipes 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

Ethanol Alcohol 75% (v/v)

Purpose

Antiseptic

Uses

Antiseptic (skin) cleanser.For personal hand hygiene to help prevent the spread of bacteria.Please close the cover and keep it sealed after use. Alcohol by nature evaporates quickly.This product is insoluble in water. Please do not put it into the toilet after use.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Warnings

For external use only.Storage in a dry place and keep away from fire or flame.When finished, snap cap shut to retain moisture.Discard wipe in trash receptacle afer use. Do not flush it down in toilet.

When Using This Product

Do not use in or contact the eyes. If contact occurs, rinse eyes throughly with water.

Keep Out Of Reach Of Children

Keep this out of reach of children.

Stop Use

Discontinue use if irritation or redness develops, if condition persists for more than 72 hours, consult with doctor.These may be signs of serious condition.If swallowed, get medical help or contact a Poison Control Center immediately.

Inactive Ingredient

Water

Package Label

50 CLOTH IN I BAG NDC: 78922-001-0180 CLOTH IN I BAG NDC: 78922-001-02100 CLOTH IN I BAG NDC: 78922-001-03100 CLOTH IN I PAIL NDC: 78922-001-04

* Please review the disclaimer below.