NDC 71089-001 Germ Free Zone Sanitizing Wipe

NDC Product Code 71089-001

NDC 71089-001-01

Package Description: 1 PACKAGE in 1 PACKAGE > 3 mL in 1 PACKAGE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Germ Free Zone Sanitizing Wipe with NDC 71089-001 is a product labeled by Germ Guards Incorporated. The generic name of Germ Free Zone Sanitizing Wipe is . The product's dosage form is and is administered via form.

Labeler Name: Germ Guards Incorporated

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.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • 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: Germ Guards Incorporated
Labeler Code: 71089
Start Marketing Date: 06-01-2017 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 - INACTIVATED, the listing data was inactivated by the FDA. 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.

Germ Free Zone Sanitizing Wipe Product Label Images

Germ Free Zone Sanitizing Wipe 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

Other

DRUG FACTS

Active Ingredient

Ethyl Alcohol 70% (v/v)

Purpose

Antimicrobia

Uses:

Helps reduce becteria, fungl, and some viruses.

Warnings

For external use only.

Otc - Do Not Use

  • Flammable, keep away from heat and flame.Do not use in or near eyes. If eye contact occurs flush thoroughly with water and seek medical care.Avoid contact with broken skin.Stop use and seek medical attention if irritation and redness occurs.Ingestion may cause alcohol poisoning, if ingested contact a physician or local poison control center.

Keep Out Of Reach Of Children.

In case of accidental ingestion, seekprofessional assistance or contact a Poison Control Center immediately.

Directions:

  • Tear open packet, wipe, discard.

Inactive Ingredients:

Purified water, Glycerol

* Please review the disclaimer below.