Aplicare Povidone-iodine Scrub

Manufacturer: Aplicare Products, LLC.
Effective date: 2020-02-03
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 23:41:58

Label at a glance#

ProductAplicare Povidone-iodine Scrub

Active ingredientPOVIDONE-IODINE

Label structure11 sections

Dosage and administration

apply locally as needed

Storage and handling

Avoid excessive heat. Store at room temperature.

Contacts and useful links#

PhoneLabel contact800-760-3236

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone-iodine USP 7.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

antiseptic skin preparation

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if allergic to iodine
in the eyes

Ask a doctor before use if injuries are

OTC - ASK DOCTOR SECTION

deep or puncture wounds
serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

STORAGE AND HANDLING SECTION

Avoid excessive heat. Store at room temperature.

Directions

DOSAGE & ADMINISTRATION SECTION

apply locally as needed

Other information

SPL UNCLASSIFIED SECTION

0.75% titratable iodine
not made with natural rubber latex
for hospital or professional use only

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

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 - 1 Swabstick Packet

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 52380-0125-1

APLICARE

◀ Tear Here Hold Upright Tear Here ▶

ONE
POVIDONE-IODINE
SCRUB SWABSTICK

ANTISEPTIC
Non-Sterile Solution

One 4-inch saturated swabstick

Reorder No. S-1112

PRINCIPAL DISPLAY PANEL - 1 Swabstick Packet

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52380-0125-1	2020-02-03	C162847	48780-1	9d75b9d0-8296-f424-e053-dadaa90a57ce	0125 Aplicare Povidone-iodine Scrub
52380-0125-1	2020-01-31	C162847	48780-1	9d75b9d0-8296-f424-e053-dadaa90a57ce	0125 Aplicare Povidone-iodine Scrub

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
52380-0125-1	EA - Each	52380-0125	70c28207-329b-4ce4-a99f-fa8f102cccaa	1	2017-07-07

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Aplicare Povidone-iodine Scrub
Povidone-iodine
SODIUM PHOSPHATE, DIBASIC
ANHYDROUS CITRIC ACID
SODIUM HYDROXIDE
NONOXYNOL-9
AMMONIUM NONOXYNOL-4 SULFATE
WATER
IODINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52380-0125	52380-0125-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM PHOSPHATE, DIBASIC	GR686LBA74	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
NONOXYNOL-9	48Q180SH9T	IACT
AMMONIUM NONOXYNOL-4 SULFATE	9HIA70O4J0	IACT
WATER	059QF0KO0R	IACT
POVIDONE-IODINE	85H0HZU99M	ACTIM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
9daf47de-49ad-a8c2-e053-2995a90a99cf			599527a2-c957-4d9b-8dfc-e9fef1516465	2020-02-03	Warnings	Exact identifier spl id: 9daf47de-49ad-a8c2-e053-2995a90a99cf spl set id: 599527a2-c957-4d9b-8dfc-e9fef1516465

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.