Ichthammol 20%

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: Ichthammol 20%
Generic name: ICHTHAMMOL
Manufacturer: TRIFECTA PHARMACEUTICALS USA LLC
Product type: HUMAN OTC DRUG
SPL set ID: 9698b98c-bca1-4a7e-8a67-05d2a2b770a5
SPL ID: 2a924831-5b30-7079-e063-6294a90a6806
Version: 12
Effective date: 2024-12-31
Source export date: 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:15:56

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Ichthammol 20%	openfda.brand_name
generic name		ICHTHAMMOL	openfda.generic_name
manufacturer name		TRIFECTA PHARMACEUTICALS USA LLC	openfda.manufacturer_name
ndc	package	69396-004-20	openfda.package_ndc
ndc	product	69396-004	openfda.product_ndc
ndc11	package	69396000420	derived:openfda.package_ndc
spl id		2a924831-5b30-7079-e063-6294a90a6806	id
spl set id		9698b98c-bca1-4a7e-8a67-05d2a2b770a5	set_id
unii		NQ14646378	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 eyes • Ask a doctor before use if you have deep puncture wounds or serious burns • Stop use and ask doctor if redness, irritation, swelling or pain persists If swallowed, get medical help or contact a Poison Control Center immediately. Before using any medication, read all label directions. Keep this carton, it contains important information.

Reported adverse events (FAERS/openFDA)#

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