Sterillium comfort

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: Sterillium comfort
Generic name: ALCOHOL
Manufacturer: BODE Chemie GmbH
Product type: HUMAN OTC DRUG
SPL set ID: 2d48dab8-f70a-a2b5-e063-6294a90a1456
SPL ID: 4cc0e8b6-8640-d9a6-e063-6294a90a9caf
Version: 2
Effective date: 2026-03-16
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:13:26

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Sterillium comfort	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		BODE Chemie GmbH	openfda.manufacturer_name
ndc	package	65616-010-21	openfda.package_ndc
ndc	package	65616-010-17	openfda.package_ndc
ndc	package	65616-010-09	openfda.package_ndc
ndc	package	65616-010-18	openfda.package_ndc
ndc	package	65616-010-20	openfda.package_ndc
ndc	package	65616-010-22	openfda.package_ndc
ndc	package	65616-010-07	openfda.package_ndc
ndc	product	65616-010	openfda.product_ndc
ndc11	package	65616001022	derived:openfda.package_ndc
ndc11	package	65616001009	derived:openfda.package_ndc
ndc11	package	65616001021	derived:openfda.package_ndc
ndc11	package	65616001018	derived:openfda.package_ndc
ndc11	package	65616001020	derived:openfda.package_ndc
ndc11	package	65616001017	derived:openfda.package_ndc
ndc11	package	65616001007	derived:openfda.package_ndc
rxcui		1041851	openfda.rxcui
spl id		4cc0e8b6-8640-d9a6-e063-6294a90a9caf	id
spl set id		2d48dab8-f70a-a2b5-e063-6294a90a1456	set_id
unii		3K9958V90M	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. Flammable, keep away from fire or flame. Do not use in or near the eyes or on mucous membranes. In case of contact, rinse thoroughly with water. 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.