NDC 0404-5988 Instant Hand Sanitizer

  1. Labeler Index
  2. Henry Schein, Inc.
  3. NDC: 0404-5988 Instant Hand Sanitizer

NDC Product Code 0404-5988

NDC CODE: 0404-5988

Proprietary Name: Instant 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 0404-5988-01

Package Description: 800 mL in 1 BOX

NDC 0404-5988-02

Package Description: 1.68 mL in 1 POUCH

NDC 0404-5988-03

Package Description: 237 mL in 1 BOTTLE, PUMP

NDC 0404-5988-04

Package Description: 473 mL in 1 BOTTLE, PUMP

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

Instant Hand Sanitizer with NDC 0404-5988 is a product labeled by Henry Schein, Inc.. The generic name of Instant Hand Sanitizer is . The product's dosage form is and is administered via form.

Labeler Name: Henry Schein, Inc.

Dosage Form: -

Product Type: 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.

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 (UNII: V5VD430YW9)
  • WATER (UNII: 059QF0KO0R)
  • TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Henry Schein, Inc.
Labeler Code: 0404
Start Marketing Date: 02-07-2012 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: E 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.

Instant Hand Sanitizer Product Label Images

Instant 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

Other

Drug Facts

Active Ingredient

Ethyl Alcohol 66.5%

Purpose

Antiseptic

Uses

  • For handwashing to decrease bacteria on skin without soap and water

Warnings

For external use only. Flammable, keep away from fire or flame

Otc - When Using

When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water

Stop Use And Ask Doctor If

  • Irritation and redness develops and persists for more than 72 hours

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • Place a small amount and rub over both hands & wrists until dry
  • Allow to dry without wiping
  • Children under 6 should be supervised while using this product

Inactive Ingredients

Aloe vera, carbomer, fragrance, purified water, triethanolamine
Distributed by HENRY SCHEIN, INC. Melville, NY 11747 USA
Made in U.S.A.

* Please review the disclaimer below.