NDC 73928-007 Anthem Hand Sanitizer

Alcohol Solution Topical - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
73928-007
Proprietary Name:
Anthem Hand Sanitizer
Non-Proprietary Name: [1]
Alcohol
Substance Name: [2]
Alcohol
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Labeler Name: [5]
    Kingkey Mbc Life Technology Group Co., Ltd
    Labeler Code:
    73928
    FDA Application Number: [6]
    part333A
    Marketing Category: [8]
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date: [9]
    07-27-2020
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Packages

    NDC Code 73928-007-01

    Package Description: 30 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-02

    Package Description: 50 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-03

    Package Description: 60 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-04

    Package Description: 100 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-05

    Package Description: 120 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-06

    Package Description: 130 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-07

    Package Description: 150 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-08

    Package Description: 160 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-09

    Package Description: 200 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-10

    Package Description: 230 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-11

    Package Description: 250 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-12

    Package Description: 260 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-13

    Package Description: 280 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-14

    Package Description: 300 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-15

    Package Description: 350 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-16

    Package Description: 380 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-17

    Package Description: 400 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-18

    Package Description: 450 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-19

    Package Description: 480 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-20

    Package Description: 500 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-21

    Package Description: 550 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-22

    Package Description: 600 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-23

    Package Description: 1000 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-24

    Package Description: 1500 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-25

    Package Description: 2000 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-26

    Package Description: 3000 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-27

    Package Description: 4000 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-28

    Package Description: 5000 mL in 1 BOTTLE, PLASTIC

    NDC Code 73928-007-29

    Package Description: 110 mL in 1 BOTTLE, PLASTIC

    Product Details

    What is NDC 73928-007?

    The NDC code 73928-007 is assigned by the FDA to the product Anthem Hand Sanitizer which is a human over the counter drug product labeled by Kingkey Mbc Life Technology Group Co., Ltd. The generic name of Anthem Hand Sanitizer is alcohol. The product's dosage form is solution and is administered via topical form. The product is distributed in 29 packages with assigned NDC codes 73928-007-01 30 ml in 1 bottle, plastic , 73928-007-02 50 ml in 1 bottle, plastic , 73928-007-03 60 ml in 1 bottle, plastic , 73928-007-04 100 ml in 1 bottle, plastic , 73928-007-05 120 ml in 1 bottle, plastic , 73928-007-06 130 ml in 1 bottle, plastic , 73928-007-07 150 ml in 1 bottle, plastic , 73928-007-08 160 ml in 1 bottle, plastic , 73928-007-09 200 ml in 1 bottle, plastic , 73928-007-10 230 ml in 1 bottle, plastic , 73928-007-11 250 ml in 1 bottle, plastic , 73928-007-12 260 ml in 1 bottle, plastic , 73928-007-13 280 ml in 1 bottle, plastic , 73928-007-14 300 ml in 1 bottle, plastic , 73928-007-15 350 ml in 1 bottle, plastic , 73928-007-16 380 ml in 1 bottle, plastic , 73928-007-17 400 ml in 1 bottle, plastic , 73928-007-18 450 ml in 1 bottle, plastic , 73928-007-19 480 ml in 1 bottle, plastic , 73928-007-20 500 ml in 1 bottle, plastic , 73928-007-21 550 ml in 1 bottle, plastic , 73928-007-22 600 ml in 1 bottle, plastic , 73928-007-23 1000 ml in 1 bottle, plastic , 73928-007-24 1500 ml in 1 bottle, plastic , 73928-007-25 2000 ml in 1 bottle, plastic , 73928-007-26 3000 ml in 1 bottle, plastic , 73928-007-27 4000 ml in 1 bottle, plastic , 73928-007-28 5000 ml in 1 bottle, plastic , 73928-007-29 110 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Anthem Hand Sanitizer?

    Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

    What are Anthem Hand Sanitizer Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Anthem Hand Sanitizer UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Anthem Hand Sanitizer Inactive Ingredients UNII Codes?

    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. The UNII codes for the inactive ingredients in this product are:

    What is the NDC to RxNorm Crosswalk for Anthem Hand Sanitizer?

    RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [6] 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.

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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.

    [12] 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".