NDC 79091-012 Hand Sanitizer Refill


NDC Product Code 79091-012

NDC 79091-012-01

Package Description: 100 mL in 1 POUCH

NDC Product Information

Hand Sanitizer Refill with NDC 79091-012 is a a human over the counter drug product labeled by Haan Brand Sl. The generic name of Hand Sanitizer Refill is alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Haan Brand Sl

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Hand Sanitizer Refill Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 70 mg/mL

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.

  • CARBOMER 934 (UNII: Z135WT9208)
  • WATER (UNII: 059QF0KO0R)
  • LIMONENE, (+)- (UNII: GFD7C86Q1W)
  • LINALOOL, (+)- (UNII: F4VNO44C09)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Haan Brand Sl
Labeler Code: 79091
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-23-2020 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Hand Sanitizer Refill 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


Uses* To decrease bacterias on the hand. Recommended for repeated use.

Uses* To decrease bacterias on the hand. Recommended for repeated use.

Active Ingredient

  • Active Ingredient PurposeEthyl Alcohol 65%...................................Antiseptic


  • For external use only- handsWhen using this product keep out o
  • F eyes. In case of contact, flush throughly with water.
  • Do Not Inhale or ingest.Avoid contact with broken skinKeep out of reach of children. In case of incidental ingestion seek professional assistance or contact a Poison Control Center inmediately.
  • Stop use and ask Doctor: if skin irritation develops.
  • Flammable: Keep away from heat and flame.

Stop Use And Ask A Doctor If

Stop use and ask a doctor if* Irritation develops

Keep Out Of Reach Of Children

Keep out of reach of children. In case of incidental ingestion, see professional advice or contact a Poison Control Center inmediately.


  • Directions: Wet hands throughly with product and allow to dry without wiping
  • For Children under 6 years of age do not use without supervision of an adult. Not recomended for infants

Inactive Ingredients

Water, Water, C10-30 Alkyl Acrylate Crosspolymer, Parfum(Fragrance), Limonene, Tromethamine, Linalool, Hexyl Cinnamal, Potassium Sorbate, Citral, Sodium Benzoate


QUESTIONS OR COMMENTS: Visit Haanready.com

* Please review the disclaimer below.