NDC 42339-001 Alcohol Prep Pad

Isopropyl Alcohol Swab Topical - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
42339-001
Proprietary Name:
Alcohol Prep Pad
Non-Proprietary Name: [1]
Isopropyl Alcohol
Substance Name: [2]
Isopropyl Alcohol
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.
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]
    Shandong Haiyan Medical Manufacture Co., Ltd.
    Labeler Code:
    42339
    FDA Application Number: [6]
    part344
    Marketing Category: [8]
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date: [9]
    02-18-2012
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Packages

    NDC Code 42339-001-01

    Package Description: 15 BOX in 1 CONTAINER / 200 SWAB in 1 BOX

    NDC Code 42339-001-02

    Package Description: 100 BOX in 1 CONTAINER / 100 SWAB in 1 BOX

    NDC Code 42339-001-03

    Package Description: 3000 SWAB in 1 CONTAINER

    NDC Code 42339-001-04

    Package Description: 100 BOX in 1 CONTAINER / 50 SWAB in 1 BOX

    NDC Code 42339-001-05

    Package Description: 30 BOX in 1 CASE / 36 SWAB in 1 BOX

    NDC Code 42339-001-06

    Package Description: 24 BOX in 1 CASE / 50 SWAB in 1 BOX

    NDC Code 42339-001-07

    Package Description: 24 BOX in 1 CASE / 100 SWAB in 1 BOX

    NDC Code 42339-001-08

    Package Description: 20 BOX in 1 CASE / 140 SWAB in 1 BOX

    NDC Code 42339-001-09

    Package Description: 30 BOX in 1 CASE / 100 SWAB in 1 BOX

    NDC Code 42339-001-10

    Package Description: 15 BOX in 1 CASE / 200 SWAB in 1 BOX

    NDC Code 42339-001-11

    Package Description: 20 BOX in 1 CASE / 200 SWAB in 1 BOX

    NDC Code 42339-001-12

    Package Description: 12 BOX in 1 CASE / 100 SWAB in 1 BOX

    NDC Code 42339-001-13

    Package Description: 48 BOX in 1 CASE / 200 SWAB in 1 BOX

    NDC Code 42339-001-14

    Package Description: 20 BOX in 1 CASE / 200 SWAB in 1 BOX

    NDC Code 42339-001-15

    Package Description: 24 BOX in 1 CASE / 400 SWAB in 1 BOX

    NDC Code 42339-001-16

    Package Description: 20 BOX in 1 CASE / 50 SWAB in 1 BOX

    NDC Code 42339-001-17

    Package Description: 20 BOX in 1 CASE / 200 SWAB in 1 BOX

    NDC Code 42339-001-18

    Package Description: 4 BOX in 1 CASE / 1000 SWAB in 1 BOX

    NDC Code 42339-001-19

    Package Description: 20 BOX in 1 CASE / 200 SWAB in 1 BOX

    NDC Code 42339-001-20

    Package Description: 10 BOX in 1 CASE / 100 SWAB in 1 BOX

    NDC Code 42339-001-21

    Package Description: 30 BOX in 1 CASE / 36 SWAB in 1 BOX

    NDC Code 42339-001-22

    Package Description: 20 BOX in 1 CASE / 80 SWAB in 1 BOX

    NDC Code 42339-001-23

    Package Description: 15 BOX in 1 CASE / 120 SWAB in 1 BOX

    NDC Code 42339-001-24

    Package Description: 20 BOX in 1 CASE / 100 SWAB in 1 BOX

    NDC Code 42339-001-25

    Package Description: 30 BOX in 1 CASE / 100 SWAB in 1 BOX

    NDC Code 42339-001-26

    Package Description: 30 BOX in 1 CASE / 140 SWAB in 1 BOX

    NDC Code 42339-001-27

    Package Description: 30 BOX in 1 CASE / 200 SWAB in 1 BOX

    NDC Code 42339-001-28

    Package Description: 96 BOX in 1 CASE / 100 SWAB in 1 BOX

    NDC Code 42339-001-29

    Package Description: 10 BOX in 1 CASE / 100 SWAB in 1 BOX

    Product Details

    What is NDC 42339-001?

    The NDC code 42339-001 is assigned by the FDA to the product Alcohol Prep Pad which is a human over the counter drug product labeled by Shandong Haiyan Medical Manufacture Co., Ltd.. The generic name of Alcohol Prep Pad is isopropyl alcohol. The product's dosage form is swab and is administered via topical form. The product is distributed in 29 packages with assigned NDC codes 42339-001-01 15 box in 1 container / 200 swab in 1 box, 42339-001-02 100 box in 1 container / 100 swab in 1 box, 42339-001-03 3000 swab in 1 container , 42339-001-04 100 box in 1 container / 50 swab in 1 box, 42339-001-05 30 box in 1 case / 36 swab in 1 box, 42339-001-06 24 box in 1 case / 50 swab in 1 box, 42339-001-07 24 box in 1 case / 100 swab in 1 box, 42339-001-08 20 box in 1 case / 140 swab in 1 box, 42339-001-09 30 box in 1 case / 100 swab in 1 box, 42339-001-10 15 box in 1 case / 200 swab in 1 box, 42339-001-11 20 box in 1 case / 200 swab in 1 box, 42339-001-12 12 box in 1 case / 100 swab in 1 box, 42339-001-13 48 box in 1 case / 200 swab in 1 box, 42339-001-14 20 box in 1 case / 200 swab in 1 box, 42339-001-15 24 box in 1 case / 400 swab in 1 box, 42339-001-16 20 box in 1 case / 50 swab in 1 box, 42339-001-17 20 box in 1 case / 200 swab in 1 box, 42339-001-18 4 box in 1 case / 1000 swab in 1 box, 42339-001-19 20 box in 1 case / 200 swab in 1 box, 42339-001-20 10 box in 1 case / 100 swab in 1 box, 42339-001-21 30 box in 1 case / 36 swab in 1 box, 42339-001-22 20 box in 1 case / 80 swab in 1 box, 42339-001-23 15 box in 1 case / 120 swab in 1 box, 42339-001-24 20 box in 1 case / 100 swab in 1 box, 42339-001-25 30 box in 1 case / 100 swab in 1 box, 42339-001-26 30 box in 1 case / 140 swab in 1 box, 42339-001-27 30 box in 1 case / 200 swab in 1 box, 42339-001-28 96 box in 1 case / 100 swab in 1 box, 42339-001-29 10 box in 1 case / 100 swab in 1 box. 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 Alcohol Prep Pad?

    Wipe injection site vigorously and discard.

    What are Alcohol Prep Pad 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 Alcohol Prep Pad UNII Codes?

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

    Which are Alcohol Prep Pad 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 Alcohol Prep Pad?

    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".