POVIDONE-IODINE PREP- povidone-iodine solution

Povidone-Iodine Prep by

Drug Labeling and Warnings

Povidone-Iodine Prep by is a Otc medication manufactured, distributed, or labeled by Owens & Minor Distribution, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Povidone-iodine USP 10%

Purpose

Antiseptic

Use

Antiseptic skin preparation

Warnings

For external use only

Do not use

if allergic to iodine
in the eyes

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  

Avoid pooling beneath patient

Avoid excessive heat. Store at room temperature.

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

 1% titratable iodine  for hospital or professional use only

Inactive ingredients

Purified water, Glycerin, Nonyl nonoxynol-10

Package Labeling:

INGREDIENTS AND APPEARANCE

POVIDONE-IODINE PREP 
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 39892-0809
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 39892-0809-1	1.5 mL in 1 PACKET; Type 0: Not a Combination Product	03/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	03/01/2019

Labeler - Owens & Minor Distribution, Inc. (847412269)