NDC 75512-002 Hs100

NDC Product Code 75512-002

NDC 75512-002-01

Package Description: 3.79 L in 1 BOTTLE, PLASTIC

NDC 75512-002-02

Package Description: 18.95 L in 1 PAIL

NDC 75512-002-03

Package Description: 208.45 L in 1 DRUM

NDC 75512-002-04

Package Description: 1023.3 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

NDC 75512-002-05

Package Description: 1231.75 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

NDC 75512-002-06

Package Description: 19684 L in 1 TANK

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

NDC Product Information

Hs100 with NDC 75512-002 is a product labeled by Integrity Bio-chemicals, 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: 1041498.

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)
  • HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
  • HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
  • 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: Integrity Bio-chemicals, Llc
Labeler Code: 75512
Start Marketing Date: 05-20-2020 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.

Hs100 Product Label Images

Hs100 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

Otc - Active Ingredient

Active Ingredient[s]  Alcohol 80% v/v

Otc - Purpose

Purpose Antiseptic

Indications & Usage

Use(s)Hand sanitizer to help reduce bacteria that potentially can causedisease. For use when soap and water are not available.

Warnings

WarningsFor external use only.  Flammable. Keep away from heat or flame.

Otc - Do Not Use

Do not use• On children less than 2 months of age• On open skin wounds

Otc - When Using

When using this product keep out of eyes, ears, and mouth. In caseof contact with eyes, rinse thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation occurs. These may be signs ofa serious condition.

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

Directions• Place enough product on hands to cover all surfaces. Rubhands together until dry.• Supervise children under 6 years of age when using theproduct to avoid swallowing.

Other Safety Information

Other information• Store between 15-30C (59-86F)• Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredient

Inactive Ingredients: glycerin, *hydroxypropyl cellulose,*hydroxypropyl methylcellulose, water*May or may not include

* Please review the disclaimer below.