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Dual Swab Scrub Swabstick by Dynarex Corporation

Medically reviewed on November 6, 2017

Dosage form: swab
Ingredients: POVIDONE-IODINE 10g in 100g
Labeler: Dynarex Corporation
NDC Code: 67777-303

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Dual Swab Povidone Iodine Prep Swabstick

Active Ingredient

Active ingredient                Purpose

Povidone iodine 10%        Antiseptic


For antiseptic application at  procedure site.

Indications and usage

For pre-operative patient skin preparation.


​For External Use Only

Avoid contact with the eyes. If contact occurs, flush with water.​​

Stop use

Stop use and ask a healthcare professional if,

  • condition worsens or persists for more than 72 hours
  • if pain, irritation, redness or swelling occurs

Ask a doctor

Ask a doctor before use if you have

  • deep puncture wounds
  • animal bites
  • serious wounds

Do not use

Do not use:

  • as a first aid antiseptic for more than 1 week
  • over large areas of the body

Keep out of reach of children

Keep out of reach of children:

  • if swallowed, get medical help or contact a Poison Control Center immediately.

Dosage and administration


For preoperative patient skin preparation:

  • Apply to procedure siteand allow to dry. Discard after single use.If not ready for immediate venipuncture, cover the area with a dry sterile gauze.

As a first aid antiseptic:

  • clean affected area
  • apply to wound once or twice daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first.

Tear at notch, remove applicator, use only once.

Inactive ingredients

Anhydrous citric acid, disodium hydrogen phosphate, Water

Other information
  • Store at room temperature
  • Avoid excessive heat

Principal Display Panel

Dynarex Dual Swab Povidone Iodine Prep Swabstick

Item #: 1210

1210 Prep.jpg

povidone iodine swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-303
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:67777-303-010.3 g in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C11/15/2015
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)
Sion Biotext Medical Ltd532775194manufacture(67777-303)

Dynarex Corporation

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.