FDA.reportPublic FDA data

Lights Povindone Iodine Scrub

Manufacturer
Lights Medical Manufacture Co., Ltd.
Effective date
2026-01-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:34:23

Label at a glance#

ProductLights Povindone Iodine Scrub
Active ingredientPOVIDONE-IODINE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Povidone-Iodine USP (7.5%)

OTC - PURPOSE SECTION

Purpose: Antiseptic

INDICATIONS & USAGE SECTION

Use:

Antiseptic skin preparation

WARNINGS SECTION

Warnings:

Do not use if allergic to iodine

For external use only

Do not use in eyes

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

OTC - ASK DOCTOR SECTION

Ask a doctor before use if injuries are

deep or puncture wounds

Serious burns

Stop use and ask a doctor if 

Redness, irritation, swelling or pain persisits or increases

Infection occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions:

Apply locally as needed.

OTHER SAFETY INFORMATION

Other information

  • Store at room temperature
  • 0.75% available iodine
  • Latax free
  • For hospital or professional use only

INACTIVE INGREDIENT SECTION

Inactive Ingredient

Citric acid, purified water, Disodium hydrogen phosphate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
314188povidone-iodine 7.5 % Topical SolutionPSN5
314188povidone-iodine 75 MG/ML Topical SolutionSCD5
314188povidone-iodine 7.5 % (titratable iodine 0.75 % ) Topical SolutionSY5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61333-205-012023-11-28C16284748780-1f386c64a-280a-0266-e053-dadaa90a7c1a61333-205
61333-205-012023-01-30C16284748780-1f386c64a-280a-0266-e053-dadaa90a7c1a61333-205

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61333-205-01Lights Povindone Iodine Scrub118 g in 1 BOTTLESOLUTION1185

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
61333-20561333-205-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
SODIUM PHOSPHATE DIBASIC DIHYDRATE94255I6E2TIACT
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
Lights Povindone Iodine ScrubPOVIDONE-IODINELights Medical Manufacture Co., Ltd.000bf57b-1805-4746-bf1c-32856241213a2026-01-21WarningsExact identifier
ndc (package): 61333-205-01
ndc (product): 61333-205
ndc11 (package): 61333020501
spl id: 48eff8fa-deee-a434-e063-6294a90aa861
spl set id: 000bf57b-1805-4746-bf1c-32856241213a

Reported adverse events (FAERS/openFDA)#

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