NDC 78829-500 Liquidproof Gel Hand Sanitizer

Alcohol

NDC Product Code 78829-500

NDC 78829-500-81

Package Description: 3785 mL in 1 JUG

NDC Product Information

Liquidproof Gel Hand Sanitizer with NDC 78829-500 is a a human over the counter drug product labeled by Four Fathers Distillery Llc. The generic name of Liquidproof Gel Hand Sanitizer is alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Four Fathers Distillery Llc

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Liquidproof Gel Hand Sanitizer 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 mL/100mL

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)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
  • WATER (UNII: 059QF0KO0R)
  • PEPPERMINT OIL (UNII: AV092KU4JH)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)

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: Four Fathers Distillery Llc
Labeler Code: 78829
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: 10-01-2020 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: 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.

Liquidproof Gel Hand Sanitizer Product Label Images

Liquidproof Gel 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

Otc - Active Ingredient

Active ingredient(s): Alcohol (ethanol) 70%.

Otc - Purpose

Purpose Antiseptic

Indications & Usage

Use(s): Helps reduce bacteria that can potentially become disease.

Warning

For external use only. FLAMMABLE: Keep away from heat and flame. DO NOT USE: On children less than 2 months of age. DO NOT USE: On open skin wounds. Keep out of eyes, ears, and mouth. Stop use if rash or irritation occurs. This could be a sign of a serious condition.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed contact doctor or poison control right away.

Dosage & Administration

Directions: Place enough product on hands to cover all surfaces, rub together until dry. Supervise children under 6 years of age to prevent swallowing.

Other Information:

Store between 59-86°f. DO NOT store in heat above 105°f. May discolor some fabrics

Inactive Ingredient

Inactive ingredient(s): Glycerin, Aloe Barbadensis Leaf Juice, Hydroxyethylcellulose, Purified Water, Essential Oils

* Please review the disclaimer below.