NDC 54555-132 Gurtler Rx Hand Sanitizer

NDC Product Code 54555-132

NDC 54555-132-01

Package Description: 3.785 L in 1 JUG

NDC 54555-132-02

Package Description: 18.9 L in 1 JUG

NDC 54555-132-03

Package Description: 208.1 L in 1 DRUM

NDC 54555-132-04

Package Description: 1040.9 L in 1 TANK

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

NDC Product Information

Gurtler Rx Hand Sanitizer with NDC 54555-132 is a product labeled by Brainerd Chemical Company Inc.,. The generic name of Gurtler Rx Hand Sanitizer is . The product's dosage form is and is administered via form.

Labeler Name: Brainerd Chemical Company Inc.,

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.

  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • HYDROGEN PEROXIDE (UNII: BBX060AN9V)
  • WATER (UNII: 059QF0KO0R)
  • LIMONENE OXIDE, TRANS-(+)- (UNII: 8VUQ1B30IK)
  • HYDROXYMETHYL CELLULOSE (UNII: 273FM27VK1)

Product Labeler Information

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

Labeler Name: Brainerd Chemical Company Inc.,
Labeler Code: 54555
Start Marketing Date: 07-01-2020 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: E - EXPIRED, the listing certification expired. 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.

Gurtler Rx Hand Sanitizer Product Label Images

Gurtler Rx 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[S]

Isopropyl alcohol 75% v/v

Purpose

Antiseptic

Use[S]

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

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

Do Not Use

  • In children less than 2 months of ageon open skin wounds

Otc - When Using

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

Otc - Stop Use

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

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 enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

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

Inactive Ingredients

Hydrogen peroxide, purified water USP, d'limonene, cocoamidopropyl betaine, hydroxypropyl methylcellulose

* Please review the disclaimer below.