53329-827 NDC - CURAD ALCOHOL PREP PADS (ISOPROPYL ALCOHOL)

Drug Information

Product NDC: 53329-827

Proprietary Name: Curad Alcohol Prep Pads

Non Proprietary Name: Isopropyl Alcohol

Active Ingredient(s):
  • 70 mL/100mL ISOPROPYL ALCOHOL


Administration Route(s): TOPICAL

Dosage Form(s): SWAB

Labeler Information

Labeler Name: Medline Industries, LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:12/19/2012

Package Information

No. Package Code Package Description Billing Unit
153329-827-091 APPLICATOR in 1 PACKET (53329-827-09) / 5 mL in 1 APPLICATOR
253329-827-2950 PACKET in 1 BOX (53329-827-29) / 1 APPLICATOR in 1 PACKET / 5 mL in 1 APPLICATOR
353329-827-30100 PACKET in 1 BOX (53329-827-30) / 1 APPLICATOR in 1 PACKET / 5 mL in 1 APPLICATOR
453329-827-3636 PACKET in 1 BOX (53329-827-36) / 1 APPLICATOR in 1 PACKET / 5 mL in 1 APPLICATOR
553329-827-40400 PACKET in 1 BOX (53329-827-40) / 1 APPLICATOR in 1 PACKET / 5 mL in 1 APPLICATOR
653329-827-60200 PACKET in 1 BOX (53329-827-60) / 1 APPLICATOR in 1 PACKET / 5 mL in 1 APPLICATOR

NDC Record

Field Name Field Value Definition
PRODUCT NDC53329-827The 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 NAMECurad Alcohol Prep PadsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXMediumA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
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 DATE12/19/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT 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 NUMBERpart333AThis 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 NAMEMedline Industries, LPName 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 STRENGTH70 
ACTIVE INGRED UNITmL/100mL 

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This page was last updated on: 2/1/2023