NDC 50685-009 Good Care Povidone Iodine Swabsticks


NDC Product Code 50685-009

NDC 50685-009-01

Package Description: 50 PACKET in 1 BOX > .7 g in 1 PACKET

NDC 50685-009-02

Package Description: 25 PACKET in 1 BOX > 1.4 g in 1 PACKET

NDC 50685-009-03

Package Description: 25 PACKET in 1 BOX > 2.1 g in 1 PACKET

NDC Product Information

Good Care Povidone Iodine Swabsticks with NDC 50685-009 is a a human over the counter drug product labeled by Dalian Goodwood Medical Care Ltd.. The generic name of Good Care Povidone Iodine Swabsticks is povidone-iodine. The product's dosage form is swab and is administered via topical form.

Labeler Name: Dalian Goodwood Medical Care Ltd.

Dosage Form: Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.

Product Type: Human Otc Drug 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.

Good Care Povidone Iodine Swabsticks Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • POVIDONE-IODINE 10 g/100g

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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Dalian Goodwood Medical Care Ltd.
Labeler Code: 50685
FDA Application Number: part333E What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 02-13-2013 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: 12-31-2021 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: N - NO 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.

Good Care Povidone Iodine Swabsticks 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 USP, 10%




  • Health-care antiseptic for preparation of the skin prior to surgeryFirst aid antiseptic to help prevent the risk of skin infection in minor cuts, scrapes, and burns


  • For external use only. Do not use or apply in the eyeson individuals who are allergic or sensitive to iodineover large areas of the bodyas a first aid antiseptic longer than 1 week unless directed by a doctor

Otc - Stop Use

Discontinue use if irritation and redness develop.Consult a doctor in case of deep or puncture wounds, animal bites, serious burns.Stop use and consult a doctor if the condition persists or gets worse.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.If swallowed, get medical help or contact a Poison Control right away


For preparation of the skin prior to surgery clean the affected area, remove swab by stick, apply to the operative site prior to surgeryFor use as a first aid antiseptic clean the affected area, apply a small amount of this product on the area 1-3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.

Other Information

  • Store at room temperature: 15 degrees - 30 degrees C (59 degrees - 86 degrees F)

Inactive Ingredients

Purified water, Povidone Iodine, Citric Acid Disodium Hydrogen Phosphate Dodecahydrate Potassium Iodate Nonoxynol

Manufactured By Dalian Goodwood Medical Care Ltd.

Made in China

* Please review the disclaimer below.