PROHEAL POVIDONE IODINE SOLUTION

Manufacturer
Click Industries LLC
Effective date
2026-09-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-10-09 01:01:48

Label at a glance#

ProductPROHEAL POVIDONE IODINE
Active ingredientPOVIDONE-IODINE
Label structure9 sections

Indications and uses

first aid to help prevent the risk of infection in: • minor cuts • scrapes • burns

Dosage and administration

• clean the affected area • apply a small amount of this product on the area 1 to 3 times daily • may be covered with a sterile bandage • if bandaged, let dry first

Storage and handling

• store at room temperature

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone-iodine, 10% (1% available iodine)

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in: • minor cuts • scrapes • burns

Warnings

WARNINGS SECTION

For external use only

Do not use
• in the eyes or apply over large areas of the body • longer than 1 week unless directed by a doctor

Ask a doctor before use in case of deep or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if condition persists or gets worse

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• clean the affected area • apply a small amount of this product on the area 1 to 3 times daily • may be covered with a sterile bandage • if bandaged, let dry first

Other information

STORAGE AND HANDLING SECTION

• store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

citric acid, disodium hydrogen phosphate, purified water.

SPL UNCLASSIFIED SECTION

PREVENTS INFECTIONS ǀ BURNS AND WOUNDS

FIRST AID ANTISEPTIC

Manufactured for:
ProHeal
Surfside, FL
www.prohealproducts.com
772-776-4325

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PH POVIDONE IODINE SOLUTIONPH POVIDONE IODINE SOLUTION

PH POVIDONE IODINE SOLUTIONPH POVIDONE IODINE SOLUTION

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeqrco.de/beBCHR86173004-6.jpg, 86173004-4.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86173-00486173-004-04, 86173-004-48, 86173-004-08, 86173-004-21, 86173-004-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-12-09full-release2026-06-01 01:28:30
12025-10-01monthly-update2026-06-03 17:38:03

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5726c295-9eb8-4483-9c49-16398cd3ab35c80f0a7c-c083-4199-a739-c9865c5cc1ef2025-12-09WarningsExact identifier
spl set id: c80f0a7c-c083-4199-a739-c9865c5cc1ef

Reported adverse events (FAERS/openFDA)#

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