NDC 52000-008 Isopropyl Rubbing Alcohol 50%

NDC Product Code 52000-008

NDC 52000-008-01

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC 52000-008-02

Package Description: 177 mL in 1 BOTTLE, PLASTIC

NDC 52000-008-03

Package Description: 237 mL in 1 BOTTLE, PLASTIC

NDC 52000-008-04

Package Description: 296 mL in 1 BOTTLE, PLASTIC

NDC 52000-008-05

Package Description: 355 mL in 1 BOTTLE, PLASTIC

NDC 52000-008-06

Package Description: 414 mL in 1 BOTTLE, PLASTIC

NDC 52000-008-07

Package Description: 473 mL in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Isopropyl Rubbing Alcohol 50% with NDC 52000-008 is product labeled by Universal Distribution Center Llc. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:

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.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Universal Distribution Center Llc
Labeler Code: 52000
Start Marketing Date: 03-13-2012 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: 12-31-2022 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Isopropyl Rubbing Alcohol 50% Product Label Images

Isopropyl Rubbing Alcohol 50% 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

Otc - Active Ingredient

Active Ingredients (by volume)Isopropyl alcohol (50% conc.)

Otc - Purpose

PurposeFirst aid antiseptic

Indications & Usage

  • Usesfirst aid to help prevent the risk of infection in minor cuts, scrapes and burns


WarningsFor external use only; flammable, keep away from fire or flame, heat, spark, electrical

Otc - Ask Doctor

  • Ask a doctor before use if you havedeep punctured wounds, animal bites or serious burns

Otc - When Using

  • When using this productdo not get into eyesdo not apply over large areas of the bodydo not use longer than one week unless directed by a doctor

Otc - Stop Use

  • Stop using this product ifcondition persists or gets worse

Otc - Keep Out Of Reach Of Children

Keep this and all drugs out of the reach of childrenIn case of accidental ingestion, seek professional assistance or contact a Poison control center (1-800-222-1212) immediately

Dosage & Administration

  • Directionsclean effected areaapply small amount of this product on the area 1-3 times dailymay be covered with a sterile bandageif bandaged, let dry first


  • Other informationstore at room temperaturedoes not contain, nor is intended as a substitute for grain or ethyl alcoholwill produce serious gastric disturbance if taken internally


Inactive Ingredient

Inactive ingredientWater(Aqua)

* Please review the disclaimer below.