FDA.reportPublic FDA data

Maokang Povidone-Iodine Scrub Solution

Manufacturer
Changzhou Maokang Medical Products Co., Ltd
Effective date
2026-01-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:34:28

Label at a glance#

ProductMaokang Povidone-Iodine Scrub
Active ingredientPOVIDONE-IODINE
Label structure7 sections

Dosage and administration

 apply locally as needed

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone-Iodine 7.5%w/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for antiseptic skin preparation

Warnings

WARNINGS SECTION

do not use

OTC - DO NOT USE SECTION

  • if allergic to Iodine
  • do not use in the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • redness,irritation,swelling or painpersists or increases
  • infection occurs   

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion,seek professional assistance or consult a poison Control Center immediately.

Avoid pooling beneath patient.

Directions

DOSAGE & ADMINISTRATION SECTION

  •  apply locally as needed

Other information

SPL UNCLASSIFIED SECTION

  •  0.75% titratable iodine
  •  for hospital or professional use only

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Anhydrous citric acid, sodium dodecyl sulfate, Nonoxynol-10, Potassium iodide, Sodium hydroxide, Purified water, Hydroxyethyl cellulose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label01.jpgLabel01.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
314188povidone-iodine 7.5 % Topical SolutionPSN1
314188povidone-iodine 75 MG/ML Topical SolutionSCD1
314188povidone-iodine 7.5 % (titratable iodine 0.75 % ) Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59050-560-01Maokang Povidone-Iodine Scrub118 mL in 1 BOTTLELIQUID1181

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59050-56059050-560-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
SODIUM LAURYL SULFATE368GB5141JIACT
NONOXYNOL-10K7O76887APIACT
POTASSIUM IODIDE1C4QK22F9JIACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
POVIDONE-IODINE85H0HZU99MACTIM

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Maokang Povidone-Iodine ScrubPOVIDONE-IODINEChangzhou Maokang Medical Products Co., Ltd5f945e64-aee7-4b68-ad8b-9c8d4875842a2026-01-20WarningsExact identifier
ndc (package): 59050-560-01
ndc (product): 59050-560
ndc11 (package): 59050056001
spl id: 48d55325-a0e3-ed8c-e063-6294a90a55d9
spl set id: 5f945e64-aee7-4b68-ad8b-9c8d4875842a

Reported adverse events (FAERS/openFDA)#

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