APLICARE POVIDONE-IODINE PREP PAD- povidone-iodine solution 
Aplicare Products, LLC

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4111 Aplicare Povidone-Iodine Prep Pad

Active Ingredient

Povidone-iodine USP 10%

Purpose

Antiseptic

Use

antiseptic skin preparation

Warnings

  • For external use only

Do not use

  • if allergic to iodine or in the eyes

Ask a doctor before use

  • if injuries are deep wounds, puncture wounds, or serious burns

Stop use and ask a doctor

  • if infection occurs or if 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.

Directions

apply locally as needed

Other Information

  • Prep pad size: 1-1/4" × 1-1/2"
  • 1% titratable iodine
  • not made with natural rubber latex
  • for hospital or professional use only
  • avoid excessive heat - store at room temperature

Inactive ingredients

citric acid, disodium phosphate, nonoxynol-9, sodium hydroxide, water

Manufacturing Information

Manufactured by:

Aplicare Products, LLC

550 Research Pkwy, Meriden CT 06450 USA

Manufactured for:

Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA with domestic and foreign materials

1-800-633-5463

RF18APL

REF: APLP1111

Package Label

Label

APLICARE POVIDONE-IODINE PREP PAD 
povidone-iodine solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52380-4111
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
NONOXYNOL-9 (UNII: 48Q180SH9T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52380-4111-10.5 mL in 1 PACKET; Type 0: Not a Combination Product05/31/201711/30/2021
2NDC:52380-4111-20.5 mL in 1 PACKET; Type 0: Not a Combination Product05/31/201711/30/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00305/31/201711/30/2021
Labeler - Aplicare Products, LLC (081054904)
Registrant - Medline Industries, LP (025460908)

Revised: 8/2023
 
Aplicare Products, LLC