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Aplicare Povidone Iodine Scrub: Package Insert / Prescribing Info

Package insert / product label
Generic name: povidone-iodine
Dosage form: topical solution
Drug classes: Antiseptic and germicides, Vaginal anti-infectives

Medically reviewed by Drugs.com. Last updated on Aug 24, 2023.

Active Ingredient

Povidone-iodine 7.5%

Purpose

Antiseptic

Indications and Usage for Aplicare Povidone Iodine Scrub

  • • antiseptic skin preparation
  • • single use when used for patient preoperative skin preparation

Warnings

  • For external use only
  • Avoid "pooling" beneath patient. Prolonged exposure to wet solution may cause skin irritation.

Do not use

  • • in the eyes
  • • on individuals allergic or sensitive to iodine

Ask a doctor before use if injuries are

  • • deep or puncture wounds
  • • serious burns

Stop use and ask a doctor if

  • • infection occurs
  • • redness, irritation, swelling or pain persists or increases

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

Aplicare Povidone Iodine Scrub Dosage and Administration

apply locally as needed

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Other information

  • • 0.75% titratable iodine
  • • not made with natural rubber latex
  • • for hospital or professional use only

Inactive ingredients

ammonium nonoxynol-4 sulfate, citric acid, disodium phosphate, nonoxynol-9, sodium hydroxide, water

Questions or comments?

1-800-633-5463

Manufacturing Information

Manufactured by:

Aplicare Products, LLC

550 Research Parkway, Meriden, CT 06450 USA

Manufactured for:

Medline Inustries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA with domestic and foreign materials

1-800-633-5463

RL17HND

REF: APL82364K

Package Label

Package Label

APLICARE POVIDONE-IODINE SCRUB
povidone-iodine solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52380-4802
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE7.5 mg in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
NONOXYNOL-9 (UNII: 48Q180SH9T)
AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0)
WATER (UNII: 059QF0KO0R)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52380-4802-8118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/1998
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/1998
Labeler - Aplicare Products, LLC (081054904)
Registrant - Medline Industries, LP (025460908)

Medical Disclaimer