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Aplicare Povidone-iodine Scrub

Medically reviewed on February 13, 2018

Dosage form: solution
Ingredients: POVIDONE-IODINE 7.5mg in 1mL
Labeler: Aplicare Products, LLC.
NDC Code: 52380-2802

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.

Aplicare Povidone-iodine Scrub

Povidone Iodine 7.5%

Antiseptic

Do not use if allergic to iodine

Do not use in eyes


Ask a doctor before use if injuries are

deep or puncture wounds

• serious burns



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

Warnings


For external use only

Avoid "pooling" beneath patient. Prolonged exposure to wet solution may cause skin irritation.

Questions or comments?

1 800-760-3236 (Monday - Friday 8:30 AM - 5:00 PM EST)

Use

• antiseptic skin preparation

• single use when used for patient preoperative skin preparation and/or preinjection indications

Directions apply locally as needed

Stop use and ask a doctor if

• infection occurs

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

Other information

• 0.75% titratable iodine

• latex free

• for hospital or professional use only

Inactive ingredients

• ammonium nonoxynol-4 sulfate

• citric acid

• disodium phosphate

• nonoxynol-9

• sodium hydroxide

• water

APLICARE

POVIDONE-IODINE SCRUB

ANTISEPTIC

NON-STERILE SOLUTION

APLICARE POVIDONE-IODINE SCRUB 
povidone-iodine solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52380-2802
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (IODINE) IODINE7.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM PHOSPHATE, DIBASIC 
ANHYDROUS CITRIC ACID 
SODIUM HYDROXIDE 
NONOXYNOL-9 
AMMONIUM NONOXYNOL-4 SULFATE 
WATER 
Packaging
#Item CodePackage Description
1NDC:52380-2802-859 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/1998
Labeler - Aplicare Products, LLC. (081054904)
Establishment
NameAddressID/FEIOperations
Aplicare Products, LLC.081054904manufacture(52380-2802), repack(52380-2802)

 
Aplicare Products, LLC.

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Further information

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

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