Povidone-Iodine Prep Pad Medium Sterile

Manufacturer
Zhejiang Xingheng Medical Supplies Co., Ltd.
Effective date
2022-08-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:50:33

Label at a glance#

ProductPovidone-Iodine Prep Pad Medium Sterile
Active ingredientPOVIDONE-IODINE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Povidone-lodine 10% w/w (equivalent to iodine 1%)

OTC - PURPOSE SECTION

Antiseptic

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

● Clean the affected area
● Apply product on the area 1-3times daily and discard
● May be covered with a sterile bandage when dry

OTC - DO NOT USE SECTION

Do not use:

  • in the eyes.
  • apply over large areas of the body.
  • on individuals who are allergic or sensitive to iodine.

OTC - STOP USE SECTION

Stop use and consult a doctor

  • if the condition persists or gets worse.
  • for use longer than 1week.

OTC - ASK DOCTOR SECTION

Ask a doctor in case of deep or puncture wounds, animal bites & serious burns.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Sodium Bicarbonate, Polysorbate 20, Polyethylene Glycol 400, Potassium Iodate, Water

DOSAGE & ADMINISTRATION SECTION

Apply topically as needed to cleanse intendend area;

Apply the product to the skin, take the injection or puncture site as the center, slowly rotate from the inside to the outside, and gradually apply the product for two times, the disinfection area should be more than 5cmx5cm, and the action time should be1min.

INDICATIONS & USAGE SECTION

Use for preparation of skin prior to injection,apply the product to the skin, take the injection or puncture site as the center, slowly rotate from the inside to the outside, and gradually apply the product for two times, the disinfection area should be more than 5cmx5cm, and the action time should be 1min.Please clean before disinfection.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Povidone-Iodine Pad 81636-006-01Povidone-Iodine Pad 81636-006-01

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81636-006-012023-07-28C16284748780-10191ceaa-6def-198a-e063-dbdaa90aec3e81636-006 Povidone-Iodine Pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81636-006-01Povidone-Iodine Prep Pad Medium Sterile100 in 1 BOXCLOTH1001
81636-006-01Povidone-Iodine Prep Pad Medium Sterile100 in 1 CARTONCLOTH1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81636-006POVIDONE-IODINE PREP PAD MEDIUM STERILE (POVIDONE-IODINE PAD) CLOTH [ZHEJIANG XINGHENG MEDICAL SUPPLIES CO., LTD.]1Legacy NDC, 2 package rows20220831_e6666508-818b-10f8-e053-2995a90a530f.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81636-00681636-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
e6666508-818c-10f8-e053-2995a90a530fe6666508-818b-10f8-e053-2995a90a530f2022-08-16WarningsExact identifier
spl id: e6666508-818c-10f8-e053-2995a90a530f
spl set id: e6666508-818b-10f8-e053-2995a90a530f

Reported adverse events (FAERS/openFDA)#

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