NDC 0924-0012 Alcohol Prep

NDC Product Code 0924-0012

NDC 0924-0012-06

Package Description: 100 PACKET in 1 BOX > .55 mL in 1 PACKET

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

NDC Product Information

Alcohol Prep with NDC 0924-0012 is a product labeled by Acme United Corporation. The generic name of Alcohol Prep is . The product's dosage form is and is administered via form.

Labeler Name: Acme United Corporation

Dosage Form: -

Product Type: 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.

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: Acme United Corporation
Labeler Code: 0924
Start Marketing Date: 01-15-2016 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: 12-31-2018 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Alcohol Prep 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 Ingredient                                       PurposeIsopropyl Alcohol 70% v/v                         Antiseptic


For preparation of the skin prior to injection.


  • For external use onlyFlammable, keep away from flame or fireNot for use with electrocautinary devices or proceduresDo not use in eyesSterile unless package is damaged or open.

Indications And Usage:

  • Stop use and ask a doctor if:Irritation or redness developscondition persists for more than 72 hoursCleansing of an injection site

Keep Out Of Reach Of Children.

In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.


Wipe injection site vigorously and discard

Other Information:

  • Store at room temperature: 15 deg C to 30 deg C   59 deg F to 86 deg Favoid excessive heat

Inactive Ingredient

  • Inactive IngredientWater

* Please review the disclaimer below.