NDC 65321-022 Foam Hand Sanitizer

NDC Product Code 65321-022

NDC CODE: 65321-022

Proprietary Name: Foam 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.

NDC Code Structure

  • 65321 - Rubbermaid Commercial Products Llc

NDC 65321-022-01

Package Description: 8 BAG in 1 CARTON > 500 mL in 1 BAG

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

NDC Product Information

Foam Hand Sanitizer with NDC 65321-022 is a product labeled by Rubbermaid Commercial Products 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: 1098198.

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)
  • SODIUM LACTATE (UNII: TU7HW0W0QT)
  • LACTIC ACID (UNII: 33X04XA5AT)

Product Labeler Information

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

Labeler Name: Rubbermaid Commercial Products Llc
Labeler Code: 65321
Start Marketing Date: 05-01-2010 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".

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Foam Hand Sanitizer Product Label Images

Foam 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 75% (v/v)

Purpose

Antiseptic

Use

  • For hand washing to decrease bacteria on skin.

Otc - Do Not Use

  • Flammable, keep away from fire or flame.For external use only.Do not ingest.Avoid contact with eyes.

Otc - Stop Use

  • Discontinue use and consult a healthcare practitioner if irritation and redness develops.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.

Inactive Ingredients

Water (Aqua), PEG-6 Caprilic/Capric Glycerides, Shea Butteramidopropyl Betaine, Disodium Lauriminodipropionate Tocopheryl Phosphates, Sodium Lactate, PEG/PPG-25/25 Dimethicone, Lactic Acid, PEG-14M

Questions?

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* Please review the disclaimer below.