PROVIDONE-IODINE PREP PADS- povidone-iodine prep pads cloth

PROVIDONE-IODINE PREP PADS by

Drug Labeling and Warnings

PROVIDONE-IODINE PREP PADS by is a Otc medication manufactured, distributed, or labeled by Yangzhou Suxiang Medical Instrument Co, LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Povidone Iodine 10%

Purpose

Antiseptic

Uses

Antiseptic cleanser to help prevent skin infection in minor cuts, scrapes, and burns

For preparation of the skin prior to surgery

Helps reduce bacteria that can potentially cause skin infection

Warnings

For External Use Only.

Do not use

In the eyes

As a first aid anticeptic for more than 1 week

Over large areas of the body

Ask a doctor before use if you have

Deep puncture wounds

Animal bites

Serious wounds

Stop use and ask a doctor if

Condition worsens or persists for more than 72 hours

Irritation and redness develops

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

Tear a notch

Remove applicator

Use only once

As a first aid antiseptic

Clean affected area

apply 1 to 3 times daily

May be covered with sterile bandage

If bandaged, let dry first

For preoperative patient skin preparation

Clean area

Apply to operative site prior to surgery using applicator

Other Information

Store at room temperature

Avoid excessive heat

Inactive Ingredients

Nonoxynol-9, water

DOSAGE & ADMINISTRATION

Sterile unless poch is opened or damaged.

Saturated with 10% Povidone Iodine.

INDICATIONS & USAGE

For External Use Only. Apply topically as needed. Discard after single use.

Povidone-Iodine Prep Pads - 200

INGREDIENTS AND APPEARANCE

PROVIDONE-IODINE PREP PADS 
povidone-iodine prep pads cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72766-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	10 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
NONOXYNOL-9 (UNII: 48Q180SH9T)

Product Characteristics
Color	brown	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72766-001-02	200 in 1 BOX; Type 0: Not a Combination Product	02/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/15/2019

Labeler - Yangzhou Suxiang Medical Instrument Co, LTD (543387280)