DURMA DynaWound Cleanser

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: DURMA DynaWound Cleanser
Generic name: WOUND CLEANSER
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 6a4dd82a-6b06-426b-9afd-415a1a4339b4
SPL ID: 4db3b7d3-81f1-d779-e063-6394a90a83df
Version: 8
Effective date: 2026-03-23
Source export date: 2026-11-06
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:04:51

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		DURMA DynaWound Cleanser	openfda.brand_name
generic name		WOUND CLEANSER	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-403-04	openfda.package_ndc
ndc	package	67777-403-02	openfda.package_ndc
ndc	package	67777-403-03	openfda.package_ndc
ndc	package	67777-403-01	openfda.package_ndc
ndc	product	67777-403	openfda.product_ndc
ndc11	package	67777040304	derived:openfda.package_ndc
ndc11	package	67777040303	derived:openfda.package_ndc
ndc11	package	67777040302	derived:openfda.package_ndc
ndc11	package	67777040301	derived:openfda.package_ndc
rxcui		582205	openfda.rxcui
spl id		4db3b7d3-81f1-d779-e063-6394a90a83df	id
spl set id		6a4dd82a-6b06-426b-9afd-415a1a4339b4	set_id
unii		PH41D05744	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 • In the eyes or over large areas of the body • Longer than 1 week unless directed by a doctor Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns. Stop use and ask a doctor if if condition persists or gets worse. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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