NDC 76088-300 Instant Hand Sanitizer Original

NDC Product Code 76088-300

NDC CODE: 76088-300

Proprietary Name: Instant Hand Sanitizer Original 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

  • 76088 - King Import Warehouse

NDC 76088-300-12

Package Description: 354 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

Instant Hand Sanitizer Original with NDC 76088-300 is a product labeled by King Import Warehouse. 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: 247835.

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)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Product Labeler Information

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

Labeler Name: King Import Warehouse
Labeler Code: 76088
Start Marketing Date: 03-02-2011 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: 12-31-2017 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.

Instant Hand Sanitizer Original Product Label Images

Instant Hand Sanitizer Original 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

Otc - Active Ingredient

Active Ingredient:Ethyl Alcohol 62.0%

Otc - Purpose

PurposeAntimicrobial

Indications & Usage

USE: hand sanitizer to help reduce bacteria on the skin that may cause disease.

Warnings

Warnings: for external use only.

Storage And Handling

Flammable. Keep away from heat and flame.

Otc - When Using

  • When using this productavoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develops.

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

  • Directionswet hands thoroughly with product and rub into skin until dry.children under 6 years of age should be supervised by an adult when using.

Inactive Ingredient

Inactive Ingredients:Water (Aqua), Triethanolamine, Carbomer, Aloe Vera Leaf Juice, Fragrance, Tocopheryl Acetate.

* Please review the disclaimer below.