NDC 52410-4150 Medpride Sterile

NDC Product Code 52410-4150

NDC 52410-4150-5

Package Description: 1000 CLOTH in 1 CASE

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

NDC Product Information

Medpride Sterile with NDC 52410-4150 is a product labeled by Shield Line Llc. The generic name of Medpride Sterile is . The product's dosage form is and is administered via form.

Labeler Name: Shield Line Llc

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)
  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)

Product Labeler Information

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

Labeler Name: Shield Line Llc
Labeler Code: 52410
Start Marketing Date: 05-27-2013 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 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.

Medpride Sterile Product Label Images

Medpride Sterile 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

Benzalkonium Chloride 0.133%

Purpose

Antiseptic

Uses

For topical antimicrobial use

Warnings

For external use only■ flammable, keep away from fire or flame

Do Not Use

■ with electrocautery procedures ■ in the eyes, if contact occurs, flush eyes with water

Stop Use And Ask A Doctor If

■if irritation and redness develops. if condition persist consult your health practitioner.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed contact a doctor or Poison Control Center right away.

Directions

■wipe the required site vigorously and discard

Other Information

■ store at room temperature 15C-30C (59F-86F)

Inactive Ingredients

Purified water, camphor

* Please review the disclaimer below.