Lights Povindone Iodine Swabstick

Manufacturer
Lights Medical Manufacture Co., Ltd.
Effective date
2026-01-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:34:30

Label at a glance#

ProductLights Povindone Iodine Swabstick
Active ingredientPOVIDONE-IODINE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Povidone-Iodine USP (10%)

Equivalent to 1% titratable Iodine

OTC - PURPOSE SECTION

Purpose: Antiseptic

INDICATIONS & USAGE SECTION

Use:

Health care antiseptic for prepapration of skin prior to surgery.

First aid antiseptic to help prevent infection in minor cuts, scrapes and burns.

WARNINGS SECTION

Warnings:

For external use only

Do not use or apply to the eyes *to individuals who are allergic or sensitive to iodine, *over large area of the body, *as first aid antiseptic longer than a week unless directed by a doctor 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or consult a poison control center right away

OTC - ASK DOCTOR SECTION

Discontinue use if irritation and redness develop. Consult a doctor iin case of deep or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if infection occurs or if condition persists or increases

DOSAGE & ADMINISTRATION SECTION

For preparation of the skin prior surgery: clean the affacted area, remove swabstick, apply to the operative site prior to surgery

For use as first aid antiseptic: clean the affacted area, apply a small anount of the product to the area 1-3 times daily. Maybe covered with a sterile bandage. If bandaged, let dry first.

OTHER SAFETY INFORMATION

Other information

  • Store at room temperature

INACTIVE INGREDIENT SECTION

Inactive Ingredient

Citric acid, disodium phosphate, purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797730povidone-iodine 10 % Medicated PadPSN3
797730povidone-iodine 100 MG/ML Medicated PadSCD3
797730povidone-iodine 10 % (titratable iodine 1 % ) Medicated PadSY3
797730povidone-iodine 10 % Medicated PadSY3
797730povidone-iodine 10 % Medicated SwabstickSY3

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
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61333-212-01Lights Povindone Iodine Swabstick1.5 g in 1 APPLICATORSWAB1.53
61333-212-01Lights Povindone Iodine Swabstick1 in 1 POUCHSWAB13

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
61333-21261333-212-01

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

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 SwabstickPOVIDONE-IODINELights Medical Manufacture Co., Ltd.977b6077-bf47-4e02-bde4-c752e73d76282026-01-21WarningsExact identifier
ndc (package): 61333-212-01
ndc (product): 61333-212
ndc11 (package): 61333021201
spl id: 48efec8f-83e7-0744-e063-6394a90a0c29
spl set id: 977b6077-bf47-4e02-bde4-c752e73d7628

Reported adverse events (FAERS/openFDA)#

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