NDC 56062-826 Publix Alcohol

NDC Product Code 56062-826

NDC 56062-826-30

Package Description: 100 PACKET in 1 BOX > 1 APPLICATOR in 1 PACKET (56062-826-09) > 5 mL in 1 APPLICATOR

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

NDC Product Information

Publix Alcohol with NDC 56062-826 is a product labeled by Lix Super Markets Inc. The generic name of Publix Alcohol is . The product's dosage form is and is administered via form.

Labeler Name: Lix Super Markets Inc

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: Lix Super Markets Inc
Labeler Code: 56062
Start Marketing Date: 01-01-2013 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: 12-31-2019 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.

Publix Alcohol 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

Active Ingredient

Isopropyl Alcohol, 70% v/v




  • For preparation of the skin prior to an injectionFirst aid to help decrease germs in minor cuts, scrapes and burns


For external use only.Flammable, keep away from fire or flame.

Do Not Use

  • With electrocautery procedureslonger than 1 week unless directed by a doctor

When Using This Product

  • Do not get into eyesdo not apply over large areas of the bodyin case of deep or puncture wounds, animal bites or serious burns, consult a doctor

Stop Use And Ask A Doctor If

  • Irritation and redness developcondition gets worse or persists for more than 72 hours

Keep Out Of Reach Of Children.

If accidentally swallowed, get medical help or contact a Poison Control Center right away.


  • Apply to skin as needed. Discard after single use.

Other Information

Protect from freezing and avoid excessive heat.

Inactive Ingredients


Package Label - Principal Display

  • PublixNDC: 56062-826-30 Sterilealcohol wipesANTISEPTICfor preparation of skin prior to injectionIsopropyl Alcohol, 70% v/vconvenient to use100 INDIVIDUALLY SEALED WIPES

* Please review the disclaimer below.