APLICARE POVIDONE-IODINE SCRUB- povidone-iodine solution
Aplicare Products, LLC

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.

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1855 7.5% PVP-I Scrub, non-sterile

Povidone-iodine USP 7.5%

Antiseptic

Use

• antiseptic skin preparation

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

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

Stop use and ask doctor if

• redness, irritation, swelling or pain persists or increases

• infection occurs

For external use only

Avoid "pooling" beneath patient

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

• 0.75% titratable iodine

• latex free

• for hospital or professional use only

Inactive ingredients

ammonium nonoxynol-4 sulfate, disodium phosphate, hydroxyethylcellulose, nonoxynol-9 phosphate, nonoxynol-10, polyoxyethylene nonylphenyl ether phosphate, water

Questions or comments?

1800 760-3236 (Monday - Friday 8:30 AM - 5:00 PM EST)

APLICARE

POVIDONE-IODINE SCRUB

ANTISEPTIC

Povidone iodine scrub

APLICARE POVIDONE-IODINE SCRUB
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:52380-1855
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	7.5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
NONOXYNOL-10 (UNII: K7O76887AP)
AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:52380-1855-2	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/20/2018	11/06/2022
2	NDC:52380-1855-4	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/20/2018	01/31/2022
3	NDC:52380-1855-8	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/20/2018	06/01/2021
4	NDC:52380-1855-6	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/20/2018	11/06/2022
5	NDC:52380-1855-3	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/20/2018	06/01/2021
6	NDC:52380-1855-7	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/20/2018	06/01/2021
7	NDC:52380-1855-9	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/20/2018	11/06/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	09/01/1998	11/06/2022

Labeler - Aplicare Products, LLC (081054904)

Registrant - Medline Industries, LP (025460908)

Revised: 11/2021

Document Id: d1f168f4-f976-e5c0-e053-2995a90a22b6

Set id: aea2c0fe-f25f-424f-827a-8fe30ad3bee0

Version: 11

Effective Time: 20211129

Aplicare Products, LLC