NDC 78186-001 Purox Hand Sanitizer

NDC Product Code 78186-001

NDC 78186-001-01

Package Description: 1.89 L in 1 BOTTLE

NDC 78186-001-02

Package Description: .384 L in 1 BOTTLE

NDC 78186-001-03

Package Description: .473 L in 1 BOTTLE

NDC 78186-001-04

Package Description: 3.785 L in 1 BOTTLE

NDC 78186-001-05

Package Description: .118 L in 1 BOTTLE

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

NDC Product Information

Purox Hand Sanitizer with NDC 78186-001 is product labeled by Purox. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:


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)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
  • 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: Purox
Labeler Code: 78186
Start Marketing Date: 07-08-2020 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.

Purox Hand Sanitizer Product Label Images

Purox 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

Alcohol 85% v/v

Purpose

Antimicrobial

Use

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from heat or flameFor external use only

Otc - When Using

  • When using this productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Otc - Stop Use

  • Stop use and ask a doctor ifirritation or rash appears and lasts.

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.

Do Not Use

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

Directions

  • Place enough product in your palm to thoroughly spread on both hands and rub into th skin until dry.Children under 6 years old should be supervised when using this product.

Other Information:

  • Store between 106F (41C)may discolor certain fabrics or surfaces

Inactive Ingredients:

Deionized Water, Aloe, Triethanolamine, Carbomer

* Please review the disclaimer below.