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

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 - 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.

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.