NDC 77388-004 Zuum 70 Ethyl Alcohol Antispetic Hand Sanitizer

  1. Labeler Index
  2. U.s. Cotton Mexico, S. De R.l. De C.v.
  3. NDC: 77388-004 Zuum 70 Ethyl Alcohol Antispetic Hand Sanitizer

NDC Product Code 77388-004

NDC CODE: 77388-004

Proprietary Name: Zuum 70 Ethyl Alcohol Antispetic Hand Sanitizer What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 77388 - U.s. Cotton Mexico, S. De R.l. De C.v.
    • 77388-004 - Zuum 70 Ethyl Alcohol Antispetic Hand Sanitizer

NDC 77388-004-01

Package Description: 420 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

Zuum 70 Ethyl Alcohol Antispetic Hand Sanitizer with NDC 77388-004 is a product labeled by U.s. Cotton Mexico, S. De R.l. De C.v.. 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.

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.
  • DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
  • 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: U.s. Cotton Mexico, S. De R.l. De C.v.
Labeler Code: 77388
Start Marketing Date: 08-01-2020 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: 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.

Zuum 70 Ethyl Alcohol Antispetic Hand Sanitizer Product Label Images

Zuum 70 Ethyl Alcohol Antispetic 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 alcohol 70%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use onlyFlammable, keep away from fire or flame

Do Not Use

In the eyes

Stop Use And Ask A Doctor If

  • Irritation and redness developcondition persists for more than 72 hours

Keep Out Of Reach Of Children.

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

Directions

Wet hands thoroughly with product and allow to dry without wiping

Other Information

  • Store between 59-86F (15-30C)Do not leave open

Inactive Ingredients

Denatonium benzoate, Water.

Questions?

800-321-1029

* Please review the disclaimer below.