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Dual Swab Scrub Swabstick by Dynarex Corporation

Dosage form: swab
Ingredients: POVIDONE-IODINE 7.5g in 100g
Labeler: Dynarex Corporation
NDC Code: 67777-302

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 Scrub Swabstick

Active Ingredient

Active ingredient                Purpose

Povidone iodine 7.5%        Antiseptic


For scrubbing procedure site, prior to antiseptic application

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:

  • scrub procedure site as required. Discard after single use and proceed to packet 2.

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

Lauramide DEA, Water

Other information
  • Store at room temperature
  • Avoid excessive heat

Principal Display Panel

Dynarex Dual Swab Povidone Iodine Scrub Swabstick

Item #: 1209

1209 Scrub.jpg

povidone iodine swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-302
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:67777-302-010.3 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(67777-302)

Dynarex Corporation

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Medically reviewed on Nov 5, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.