NDC 41520-558 Salicylic Acid

NDC Product Code 41520-558

NDC CODE: 41520-558

Proprietary Name: Salicylic Acid What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used on the skin to treat common skin and foot (plantar) warts. Salicylic acid helps cause the wart to gradually peel off. This medication is also used to help remove corns and calluses. This product should not be used on the face or on moles, birthmarks, warts with hair growing from them, or genital/anal warts. Salicylic acid is a keratolytic. It belongs to the same class of drugs as aspirin (salicylates). It works by increasing the amount of moisture in the skin and dissolving the substance that causes the skin cells to stick together. This makes it easier to shed the skin cells. Warts are caused by a virus. Salicylic acid does not affect the virus.

NDC Code Structure

  • 41520 - Foodhold Usa

NDC 41520-558-09

Package Description: 9 PATCH in 1 PACKAGE

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

NDC Product Information

Salicylic Acid with NDC 41520-558 is a product labeled by Foodhold Usa. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 240559.

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.

  • POLYVINYL ACETATE (UNII: 32K497ZK2U)
  • VINYL ACETATE (UNII: L9MK238N77)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)

Product Labeler Information

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

Labeler Name: Foodhold Usa
Labeler Code: 41520
Start Marketing Date: 11-27-2017 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: 12-31-2021 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".

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Salicylic Acid Product Label Images

Salicylic Acid 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

Salicylic acid 40%

Purpose

Corn remover

Uses

  • For the removal of cornsrelieves pain by removing corns

Warnings

For external use only.

Do Not Use

  • If you are diabetichave poor blood circulationon irritated skin, or any area that is infected or reddened

Otc - Ask Doctor

Stop use and ask a doctor if discomfort persists

Keep Out Of Reach Of Children.

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

Directions

  • Wash affected area and dry area thoroughlyif necessary, cut medicated patch to fit cornapply adhesive side down of medicated patch onto corncover medicated patch with padafter 48 hours, remove medicated patchrepeat procedure every 48 hours as needed for up to 14 days (until corn is removed)may soak corn in warm water for 5 minutes to assist in removal

Other Information

Store between 15°C to 30°C (59°F to 86°F)

Inactive Ingredients

Acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

Call 1-866-964-0939

* Please review the disclaimer below.