FDA.reportPublic FDA data

Povidone-lodine prep pad

Manufacturer
SHENZHEN BENLIJU BIO-TECH CO.,LTD
Effective date
2026-01-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:31:10

Label at a glance#

ProductPovidone-lodine prep pad
Active ingredientPOVIDONE-IODINE
Label structure12 sections

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Available Iodine

OTC - PURPOSE SECTION

disinfect

INDICATIONS & USAGE SECTION

For preparation of the skin prior to an injection and to decrease germs in minor cuts and scrapes.

WARNINGS SECTION

*For extemal use only.
*Flammable. keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use " with electrocautery procedures " in the eyes. lf contact occurs, flush eyes with water.

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

*Stop use if irritation and redness develop. If condition persists consult your health care practioner.

*Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

DOSAGE & ADMINISTRATION SECTION

For preparation of the skin prior to an injection and to decrease germs in minor cuts and scrapes.One piece at a time.

STORAGE AND HANDLING SECTION

Store at room temperature.

INACTIVE INGREDIENT SECTION

water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKINGPACKING

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
84449-002-01Povidone-lodine prep pad1 g in 1 PATCHPATCH13

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84449-00284449-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
POVIDONE-IODINE85H0HZU99MACTIM
WATER059QF0KO0RIACT

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
Povidone-lodine prep padPOVIDONE-LODINE PREP PADSHENZHEN BENLIJU BIO-TECH CO.,LTD201545b8-0697-5601-e063-6394a90a12f42026-01-05WarningsExact identifier
ndc (package): 84449-002-01
ndc (product): 84449-002
ndc11 (package): 84449000201
spl id: 479e3fc6-918d-5eb5-e063-6394a90ae933
spl set id: 201545b8-0697-5601-e063-6394a90a12f4

Reported adverse events (FAERS/openFDA)#

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