Antiseptic Patient Preoperative Skin Preparation and Surgical Hand Scrub

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Antiseptic Patient Preoperative Skin Preparation and Surgical Hand Scrub
Generic name: POVIDONE-IODINE
Manufacturer: Degasa SA De CV
Product type: HUMAN OTC DRUG
SPL set ID: 90a228bc-f380-4bc6-ae65-957c66e59b3c
SPL ID: 09735b00-e29b-ab1f-e063-6294a90a81ea
Version: 5
Effective date: 2023-11-05
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:32:20

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Antiseptic Patient Preoperative Skin Preparation and Surgical Hand Scrub	openfda.brand_name
generic name		POVIDONE-IODINE	openfda.generic_name
manufacturer name		Degasa SA De CV	openfda.manufacturer_name
ndc	package	67326-352-05	openfda.package_ndc
ndc	package	67326-352-03	openfda.package_ndc
ndc	package	67326-352-06	openfda.package_ndc
ndc	package	67326-352-07	openfda.package_ndc
ndc	package	67326-352-08	openfda.package_ndc
ndc	product	67326-352	openfda.product_ndc
ndc11	package	67326035205	derived:openfda.package_ndc
ndc11	package	67326035208	derived:openfda.package_ndc
ndc11	package	67326035203	derived:openfda.package_ndc
ndc11	package	67326035207	derived:openfda.package_ndc
ndc11	package	67326035206	derived:openfda.package_ndc
rxcui		211747	openfda.rxcui
spl id		09735b00-e29b-ab1f-e063-6294a90a81ea	id
spl set id		90a228bc-f380-4bc6-ae65-957c66e59b3c	set_id
unii		85H0HZU99M	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: For External Use Only Do not use Stop use and ask a doctor if In the eyes Heat prior to application On individuals who are allergic or sensitive to Iodine Irritation and redness develop If condition persists for more than 72 hous consult a doctor Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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