NDC 0363-0939 Apothecary Pvp Topical

NDC Product Code 0363-0939

NDC 0363-0939-08

Package Description: 236 mL in 1 BOTTLE

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

NDC Product Information

Apothecary Pvp Topical with NDC 0363-0939 is a product labeled by Walgreen Company. The generic name of Apothecary Pvp Topical is . The product's dosage form is and is administered via form.

Labeler Name: Walgreen Company

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.

  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T)
  • NONOXYNOL-9 (UNII: 48Q180SH9T)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • 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: Walgreen Company
Labeler Code: 0363
Start Marketing Date: 06-13-2011 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: 12-31-2017 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.

Apothecary Pvp Topical 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

Povidone-Iodine, 10% (equivalent to 1% available iodine)

Purpose

Antiseptic

Uses

First aid antiseptic to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only.

Do Not Use

  • In the eyeslonger than one week unless directed by a doctoron individuals who are allergic or sensitive to iodineor apply over large areas of the body

Stop Use And Ask A Doctor

  • If irritation and redness developif condition persists for more than 72 hoursin case of deep or puncture wounds, animal bites or serious burns.

Keep Out Of Reach Of Children.

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

Directions

  • Clean the affected area.Apply a small amount of this product on the area 1 to 3 times dailyMay be covered with a sterile bandage. If bandaged, let dry first.

Other Information

Protect from freezing. Avoid excessive heat.

Inactive Ingredients

Citric Acid, Disodium Phosphate, Nonoxynol-9, Sodium Hydroxide, Water.

* Please review the disclaimer below.