NDC 79883-010 Hand Sanitizer Christmas Memories

Isopropyl Alcohol

NDC Product Code 79883-010

NDC 79883-010-01

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC 79883-010-02

Package Description: 120 mL in 1 BOTTLE, PLASTIC

NDC 79883-010-03

Package Description: 250 mL in 1 BOTTLE, PLASTIC

NDC 79883-010-04

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC 79883-010-05

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC 79883-010-06

Package Description: 120 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Hand Sanitizer Christmas Memories with NDC 79883-010 is a a human over the counter drug product labeled by Taicorp Enterprises Limited. The generic name of Hand Sanitizer Christmas Memories is isopropyl alcohol. The product's dosage form is spray and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1014638.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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 Christmas Memories 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.

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.

  • CLOVE OIL (UNII: 578389D6D0)
  • WATER (UNII: 059QF0KO0R)

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.

Product Labeler Information

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

Labeler Name: Taicorp Enterprises Limited
Labeler Code: 79883
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: 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: N - NO 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.

Hand Sanitizer Christmas Memories Product Label Images

Hand Sanitizer Christmas Memories 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

Isopropyl alcohol 70% v/v




To help reduce bacteria on the skin.


  • For external use only.Flammability warning. Keep away from heat or flame.Do not useon children less than 2 years of age (unless directed by a doctor).When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.Stop use and consult a doctor if irritation develops.

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.


  • Dispense enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry.

Inactive Ingredients

Aloe Vera Extract, Cinnamon Essential Oil, Clove Essential Oil, Ginger Essential Oil, Glycerin, Sweet Orange Essential Oil, Vanilla Essential Oil, Water.

* Please review the disclaimer below.