FDA.reportPublic FDA data

Lightning X Iodine Prep Pads - Changzhou Maokang Medical Products Co., Ltd.

Manufacturer
Changzhou Maokang Medical Products Co., Ltd.
Effective date
2026-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:56:17

Label at a glance#

ProductLightning X Iodine Prep Pads
Active ingredientPOVIDONE-IODINE
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

dosagedosage

WARNINGS SECTION

warningwarning

INACTIVE INGREDIENT SECTION

inactive ingredientinactive ingredient

INDICATIONS & USAGE SECTION

indicationindication

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out the reach of childrenkeep out the reach of children

OTC - PURPOSE SECTION

purposepurpose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797730povidone-iodine 10 % Medicated PadPSN1
797730povidone-iodine 100 MG/ML Medicated PadSCD1
797730povidone-iodine 10 % (titratable iodine 1 % ) Medicated PadSY1
797730povidone-iodine 10 % Medicated PadSY1
797730povidone-iodine 10 % Medicated SwabstickSY1

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
59050-121-01Lightning X Iodine Prep Pads5.5 g in 1 POUCHPATCH5.51

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59050-12159050-121-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM HYDROXIDE55X04QC32IIACT
HYDROXYETHYL CELLULOSE (140 CPS AT 5%)8136Y38GY5IACT
GLYCERINPDC6A3C0OXIACT
POVIDONE-IODINE85H0HZU99MACTIM
POTASSIUM IODIDE1C4QK22F9JIACT
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
Lightning X Iodine Prep PadsPOVIDONE-IODINEChangzhou Maokang Medical Products Co., Ltd.5136a99b-ef40-937e-e063-6394a90a0a952026-05-07WarningsExact identifier
ndc (package): 59050-121-01
ndc (product): 59050-121
ndc11 (package): 59050012101
spl id: 5136a99b-ef41-937e-e063-6394a90a0a95
spl set id: 5136a99b-ef40-937e-e063-6394a90a0a95

Reported adverse events (FAERS/openFDA)#

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