Healther Providers Data Logo

42339-001 NDC - ALCOHOL PREP PAD (ISOPROPYL ALCOHOL)

Drug Information

Product NDC: 42339-001

Proprietary Name: Alcohol Prep Pad

Non Proprietary Name: Isopropyl Alcohol

Active Ingredient(s):
  • .7 mL/1 ISOPROPYL ALCOHOL


Administration Route(s): TOPICAL

Dosage Form(s): SWAB

Labeler Information

Labeler Name: Shandong Haiyan Medical Manufacture Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part344
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:2/18/2012

Package Information

No. Package Code Package Description Billing Unit
142339-001-0115 BOX in 1 CONTAINER (42339-001-01) / 200 SWAB in 1 BOX
242339-001-02100 BOX in 1 CONTAINER (42339-001-02) / 100 SWAB in 1 BOX
342339-001-033000 SWAB in 1 CONTAINER (42339-001-03)
442339-001-04100 BOX in 1 CONTAINER (42339-001-04) / 50 SWAB in 1 BOX
542339-001-0530 BOX in 1 CASE (42339-001-05) / 36 SWAB in 1 BOX
642339-001-0624 BOX in 1 CASE (42339-001-06) / 50 SWAB in 1 BOX
742339-001-0724 BOX in 1 CASE (42339-001-07) / 100 SWAB in 1 BOX
842339-001-0820 BOX in 1 CASE (42339-001-08) / 140 SWAB in 1 BOX
942339-001-0930 BOX in 1 CASE (42339-001-09) / 100 SWAB in 1 BOX
1042339-001-1015 BOX in 1 CASE (42339-001-10) / 200 SWAB in 1 BOX
1142339-001-1120 BOX in 1 CASE (42339-001-11) / 200 SWAB in 1 BOX
1242339-001-1212 BOX in 1 CASE (42339-001-12) / 100 SWAB in 1 BOX
1342339-001-1348 BOX in 1 CASE (42339-001-13) / 200 SWAB in 1 BOX
1442339-001-1420 BOX in 1 CASE (42339-001-14) / 200 SWAB in 1 BOX
1542339-001-1524 BOX in 1 CASE (42339-001-15) / 400 SWAB in 1 BOX
1642339-001-1620 BOX in 1 CASE (42339-001-16) / 50 SWAB in 1 BOX
1742339-001-1720 BOX in 1 CASE (42339-001-17) / 200 SWAB in 1 BOX
1842339-001-184 BOX in 1 CASE (42339-001-18) / 1000 SWAB in 1 BOX
1942339-001-1920 BOX in 1 CASE (42339-001-19) / 200 SWAB in 1 BOX
2042339-001-2010 BOX in 1 CASE (42339-001-20) / 100 SWAB in 1 BOX
2142339-001-2130 BOX in 1 CASE (42339-001-21) / 36 SWAB in 1 BOX
2242339-001-2220 BOX in 1 CASE (42339-001-22) / 80 SWAB in 1 BOX
2342339-001-2315 BOX in 1 CASE (42339-001-23) / 120 SWAB in 1 BOX
2442339-001-2420 BOX in 1 CASE (42339-001-24) / 100 SWAB in 1 BOX
2542339-001-2530 BOX in 1 CASE (42339-001-25) / 100 SWAB in 1 BOX
2642339-001-2630 BOX in 1 CASE (42339-001-26) / 140 SWAB in 1 BOX
2742339-001-2730 BOX in 1 CASE (42339-001-27) / 200 SWAB in 1 BOX
2842339-001-2896 BOX in 1 CASE (42339-001-28) / 100 SWAB in 1 BOX
2942339-001-2910 BOX in 1 CASE (42339-001-29) / 100 SWAB in 1 BOX

NDC Record

Field Name Field Value Definition
PRODUCT NDC42339-001The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEAlcohol Prep PadThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEIsopropyl AlcoholThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESWABThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/18/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct 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.
APPLICATION NUMBERpart344This 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.
LABELER NAMEShandong Haiyan Medical Manufacture Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEISOPROPYL ALCOHOLAn 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.
ACTIVE NUMERATOR STRENGTH.7 
ACTIVE INGRED UNITmL/1 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023
« Previous Code
Next Code »