Povidone Iodine Swabsticks 4 Triple

Manufacturer
Amsino healthcare (USA) inc.
Effective date
2023-11-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:59:50

Label at a glance#

ProductPovidone Iodine Swabsticks 4 Triple
Active ingredientPOVIDONE-IODINE
Label structure7 sections

Dosage and administration

apply locally as needed

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone-lodine USP10%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for antiseptic skin preparation

Warnings

WARNINGS SECTION

  • do not use if allergic to iodine
  • do not use in the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • redness,irritation,swelling or pain persists or increases
  • infection occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Avoid pooling beneath patient.

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

injuries are

For external use only.

  • deep or puncture wounds
  • serious burns

Directions

DOSAGE & ADMINISTRATION SECTION

apply locally as needed

Other information

SPL UNCLASSIFIED SECTION

  • 1% titratable iodine
  • For hospital or professional use only
  • Store at room temperature.
  • Avoid excessive heat.
  • Not made with natural rubber latex.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Citric Acid,Alkyl Glucoside,Hydroxyethyl Cellulose,Nonoxynol-10,Glycerin,Sodium Hydroxide,Potassium lodide,Purified Water.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1300277povidone-iodine gel 10 % Medicated PadPSN2
1300277povidone-iodine 0.1 MG/MG Medicated PadSCD2
1300277povidone-iodine 10 % (titratable iodine 1 % ) Gel SwabstickSY2
1300277povidone-iodine 10 % Gel SwabstickSY2
1300277povidone-iodine 10 % SwabstickSY2

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
72838-0360-1Povidone Iodine Swabsticks 4 Triple2 g in 1 APPLICATORSWAB22
72838-0360-1Povidone Iodine Swabsticks 4 Triple3 in 1 POUCHSWAB32

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72838-0360POVIDONE IODINE SWABSTICKS 4 TRIPLE (POVIDONE-IODINE) SWAB [AMSINO HEALTHCARE (USA) INC.]2Current NDC, Legacy NDC, 2 package rows20231111_45fdd9e3-031f-4741-868d-da606f60bb5a.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72838-036072838-0360-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
Povidone Iodine Swabsticks 4 TriplePOVIDONE-IODINEAmsino healthcare (USA) inc.45fdd9e3-031f-4741-868d-da606f60bb5a2023-11-10WarningsExact identifier
ndc (package): 72838-0360-1
ndc (product): 72838-0360
ndc11 (package): 72838036001
spl id: 09c727e0-0190-4b43-e063-6394a90abe69
spl set id: 45fdd9e3-031f-4741-868d-da606f60bb5a

Reported adverse events (FAERS/openFDA)#

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