APLICARE POVIDONE-IODINE SCRUB LARGE WING SPONGE- povidone-iodine scrub solution

Aplicare Povidone-iodine Scrub Large Wing Sponge by

Drug Labeling and Warnings

Aplicare Povidone-iodine Scrub Large Wing Sponge by is a Otc medication manufactured, distributed, or labeled by Aplicare, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Povidone-iodine USP 10%

Purpose

Antiseptic

Use

• antiseptic skin preparation

Warnings

Do not use

• if allergic to iodine
• in the eyes

Ask a doctor before use if injuries are

• deep wounds
• puncture wounds
• serious burns

Stop use and ask a doctor if

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

For external use only

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

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

Avoid excessive heat. Store at room temperature.

Directions

use sponges to prep desired area

Other information

• 1% titratable iodine
• for single use only
• not made with natural rubber latex
• for hospital or professional use only

Inactive ingredients

ammonium nonoxynol-4 sulfate, citric acid, disodium phosphate, nonoxynol-9, sodium hydroxide, water

QUESTIONS

For questions, comments, or to report serious side effects:
800-760-3236
Monday-Friday 8:30 a.m.-5:00 p.m. EST

PRINCIPAL DISPLAY PANEL - 2 Sponge Packet

NDC: 52380-0124-2

APLICARE

◀ Tear Here   Hold Upright   Tear Here ▸

TWO POVIDONE-IODINE SCRUB
LARGE WINGED SPONGES

ANTISEPTIC
Non-Sterile Solution

Two Large Winged Sponges Saturated with
Povidone-Iodine Scrub USP

Reorder No. F-2012

INGREDIENTS AND APPEARANCE

APLICARE POVIDONE-IODINE SCRUB LARGE WING SPONGE 
povidone-iodine scrub solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52380-0124
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
NONOXYNOL-9 (UNII: 48Q180SH9T)
AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52380-0124-2	120 mL in 1 PACKET; Type 0: Not a Combination Product	05/31/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/31/2017

Labeler - Aplicare, Inc. (107255002)

Establishment
Name	Address	ID/FEI	Business Operations
Aplicare, Inc.		107255002	manufacture(52380-0124)