Dynarex Povidone Iodine Prep Solution

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: Dynarex Povidone Iodine Prep Solution
Generic name: POVIDONE IODINE PREP SOLUTION
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 6bb4d55b-2be7-3549-e053-2a91aa0a2bb0
SPL ID: 275871a0-3173-c7fa-e063-6394a90ac014
Version: 6
Effective date: 2024-11-20
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/3744b3ae389d13e8f30cade845ea29e0fc75bb043dcda980c2025693f0c10522/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 09:05:53

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Dynarex Povidone Iodine Prep Solution	openfda.brand_name
generic name		POVIDONE IODINE PREP SOLUTION	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-141-41	openfda.package_ndc
ndc	package	67777-141-51	openfda.package_ndc
ndc	package	67777-141-50	openfda.package_ndc
ndc	package	67777-141-60	openfda.package_ndc
ndc	package	67777-141-31	openfda.package_ndc
ndc	package	67777-141-40	openfda.package_ndc
ndc	package	67777-141-61	openfda.package_ndc
ndc	package	67777-141-30	openfda.package_ndc
ndc	product	67777-141	openfda.product_ndc
ndc11	package	67777014131	derived:openfda.package_ndc
ndc11	package	67777014140	derived:openfda.package_ndc
ndc11	package	67777014151	derived:openfda.package_ndc
ndc11	package	67777014130	derived:openfda.package_ndc
ndc11	package	67777014150	derived:openfda.package_ndc
ndc11	package	67777014161	derived:openfda.package_ndc
ndc11	package	67777014160	derived:openfda.package_ndc
ndc11	package	67777014141	derived:openfda.package_ndc
rxcui		312564	openfda.rxcui
spl id		275871a0-3173-c7fa-e063-6394a90ac014	id
spl set id		6bb4d55b-2be7-3549-e053-2a91aa0a2bb0	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 if allergic to iodine in the eyes Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours 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.