NDC 79566-001 Vax-man Antiseptic Hand Wipes

Alcohol

NDC Product Code 79566-001

NDC 79566-001-01

Package Description: 1 PACKET in 1 PACKET > 4.8 mL in 1 PACKET

NDC 79566-001-02

Package Description: 50 POUCH in 1 POUCH > 240 mL in 1 POUCH

NDC 79566-001-03

Package Description: 80 POUCH in 1 POUCH > 384 mL in 1 POUCH

NDC 79566-001-04

Package Description: 100 POUCH in 1 POUCH > 480 mL in 1 POUCH

NDC 79566-001-05

Package Description: 80 CANISTER in 1 CANISTER > 150 mL in 1 CANISTER

NDC 79566-001-06

Package Description: 100 CANISTER in 1 CANISTER > 150 mL in 1 CANISTER

NDC 79566-001-07

Package Description: 140 CANISTER in 1 CANISTER > 210 mL in 1 CANISTER

NDC 79566-001-08

Package Description: 200 CANISTER in 1 CANISTER > 420 mL in 1 CANISTER

NDC 79566-001-09

Package Description: 400 CONTAINER in 1 CONTAINER > 840 mL in 1 CONTAINER

NDC 79566-001-10

Package Description: 500 CONTAINER in 1 CONTAINER > 1050 mL in 1 CONTAINER

NDC 79566-001-11

Package Description: 750 CONTAINER in 1 CONTAINER > 1575 mL in 1 CONTAINER

NDC Product Information

Vax-man Antiseptic Hand Wipes with NDC 79566-001 is a a human over the counter drug product labeled by Vaxman Group 2015 Ltd.. The generic name of Vax-man Antiseptic Hand Wipes is alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Vaxman Group 2015 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.

Vax-man Antiseptic Hand 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 70 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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • LACTIC ACID (UNII: 33X04XA5AT)

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: Vaxman Group 2015 Ltd.
Labeler Code: 79566
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: 07-10-2020 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.

Vax-man Antiseptic Hand Wipes Product Label Images

Vax-man Antiseptic Hand 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 Ingredients

Alcohol 70% v/v

Purpose

Antiseptic

Uses

  • Sanitizing wipe to help reduce bacteria that potentially can cause diseasefor use when soap and water are not availablesafe for repeated use

Warnings

For external use only.Flammable. Keep away from heat or flame.

Do Not Use

As a diaper wipe

When Using This Product

Avoid contact with eyes. If contact occurs, flush thoroughly with water.

Discontinue Use

If irritation or redness develops. If condition persists for more than 72 hours contact a doctor.

Keep Out Of Reach Of Children

Unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Open the plastic cap. Open reusable sticker label. Pull up first wipe. Reseal sticker label and close plastic cap. Discard wipe in trash receptacle after use. Do not flush.

Other Information

Store in a cool, dry place, away from direct sunlightContact: 415 Ocean Parkway Apt 2g. Brooklyn NY 11218

Inactive Ingredients

Water, Aloe Barbadensis Leaf Juice, Glycerin, Potassium Sorbate, Sodium Benzoate, Fragrance, Lactic Acid.

Company Information

Vaxman Group 2015 LtdHaifa Israelvaxmangroup@gmail.comwww.vaxmangroupcomMade in Israel

Product Packaging - 200 Wipe Canister

Vax-Man Antiseptic Hand WipesFor a better world70% Alcohol200 WIPES

* Please review the disclaimer below.