NDC 50332-0047 Pvp Iodine

NDC Product Code 50332-0047

NDC 50332-0047-0

Package Description: 10 PACKET in 1 BOX > .35 g in 1 PACKET

NDC 50332-0047-7

Package Description: 100 PACKET in 1 BOX > .35 g in 1 PACKET

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

NDC Product Information

Pvp Iodine with NDC 50332-0047 is a product labeled by Hart Health. The generic name of Pvp Iodine is . The product's dosage form is and is administered via form.

Labeler Name: Hart Health

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 ACETATE (UNII: DSO12WL7AU)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • 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: Hart Health
Labeler Code: 50332
Start Marketing Date: 04-01-1974 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: 12-31-2020 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.

Pvp Iodine 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% titratable iodine)

Purpose

Topical Antiseptic

Uses

  • First aid topical antiseptic to help prevent infection in:minor cutsscrapesburnsabrasions

Warnings

For external use only

Do Not Use

  • In the eyes or over large portions of the bodyon serious burnson animal biteson deep or puncture wounds

Stop Use And Ask A Doctor If

  • Symptoms last more than 72 hoursredness, swelling, irritation or pain occurs

Keep Out Of Reach Of Children

If swallowed get medical help or contact a Poison Control Center right away 1-800-222-1222

Directions

  • Adults and children 12 years of age and over:apply topically to clean affected area 1 to 3 times dailywhen dry, may be covered with a sterile bandageif gets in eyes, flush thoroughly with waterChildren under 12 years of age:ask a doctor

Inactive Ingredients

Citric Acid, Glyercin, Nonoxynol, Sodium Hydroxide, Water

* Please review the disclaimer below.