NDC 67618-153 Betadine Solution Swabsticks

NDC Product Code 67618-153

NDC 67618-153-01

Package Description: 1 SWAB in 1 PACKET

NDC 67618-153-03

Package Description: 3 SWAB in 1 PACKET

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

NDC Product Information

Betadine Solution Swabsticks with NDC 67618-153 is a product labeled by Purdue Products Lp. The generic name of Betadine Solution Swabsticks is . The product's dosage form is and is administered via form.

Labeler Name: Purdue Products Lp

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.

  • NONOXYNOL-9 (UNII: 48Q180SH9T)
  • 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: Purdue Products Lp
Labeler Code: 67618
Start Marketing Date: 09-15-1972 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: 12-31-2018 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.

Betadine Solution 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

Drug Facts

Active Ingredient PurposePovidone-iodine Solution USP, 10% (equal to 1% available iodine)




  • For preparation of the skin prior to surgeryhelps reduce bacteria that can potentially cause skin infection


For external use only

Do Not Use This Product

  • In the eyesif you are allergic to iodine or other product ingredients

When Using This Product

  • Prolonged exposure may cause irritation or, rarely, severe skin reactions

Stop Using This Product

  • In rare instances of local irritation or sensitivityif irritation and redness develop and continue for more than 72 hours


  • Tear at slit; pull top of packette across, exposing end of swabstickremove Betadine Solution Swabstick and apply as neededuse one time only

Other Information

  • Store between 20°-25°C (68°-77°F)Avoid freezing and excessive heat above 40°C (104°F)

Inactive Ingredients

Citric acid, disodium phosphate, nonoxynol-9, purified water, sodium hydroxide

* Please review the disclaimer below.