NDC 69221-501 Zoono Ultra Hand Sanitizer

NDC Product Code 69221-501

NDC 69221-501-01

Package Description: 150 mL in 1 BOTTLE

NDC 69221-501-02

Package Description: 50 mL in 1 BOTTLE

NDC 69221-501-11

Package Description: 50 mL in 1 BOTTLE

NDC 69221-501-13

Package Description: 150 mL in 1 BOTTLE

NDC 69221-501-15

Package Description: 1000 mL in 1 BOTTLE

NDC 69221-501-16

Package Description: 3785 mL in 1 BOTTLE

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

NDC Product Information

Zoono Ultra Hand Sanitizer with NDC 69221-501 is a product labeled by Zoono Usa, Llc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 582753.

Zoono Ultra Hand Sanitizer 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.


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: Zoono Usa, Llc
Labeler Code: 69221
Start Marketing Date: 11-14-2016 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: 12-31-2020 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.

Zoono Ultra Hand Sanitizer Product Label Images

Zoono Ultra Hand Sanitizer 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 Alchol 70%

Purpose

Antiseptic

Uses

For personal hand sanitizing and to reduce bacteria on the skin. Recommended for repeated use.

Warnings

For external use only.Do not use in the eyes.

When Using This Product

Avoid contact with eyes. In case of eye contact flush eyes with water.

Stop Use And Ask A Doctor If

Irritation and redness develop.

Keep Out Of Reach Of Children.

If swallowed get medical help or contact a Poison Control Cener right away.

Directions

Apply liberally to the hands and gently rub until dry.

Inactive Ingredients

Alcohol, Benzalkonium chloride, Fragrance, Polysorbate, Silica Complex 3-(Trimethoxysilyl) Propyl Dimethyl Octadecyl Ammonium Chloride, Water

* Please review the disclaimer below.