Ecolab

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: Ecolab
Generic name: ETHYL ALCOHOL
Manufacturer: Ecolab Inc.
Product type: HUMAN OTC DRUG
SPL set ID: f30e801c-d7ae-4a6f-830b-31d86c4f5b8c
SPL ID: 36a95f34-15a5-4a79-ad9d-c7ec35968bb0
Version: 5
Effective date: 2024-04-26
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 02:09:24

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		Ecolab	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		Ecolab Inc.	openfda.manufacturer_name
ndc	package	47593-489-26	openfda.package_ndc
ndc	package	47593-489-31	openfda.package_ndc
ndc	package	47593-489-55	openfda.package_ndc
ndc	package	47593-489-49	openfda.package_ndc
ndc	package	47593-489-33	openfda.package_ndc
ndc	product	47593-489	openfda.product_ndc
ndc11	package	47593048949	derived:openfda.package_ndc
ndc11	package	47593048931	derived:openfda.package_ndc
ndc11	package	47593048933	derived:openfda.package_ndc
ndc11	package	47593048955	derived:openfda.package_ndc
ndc11	package	47593048926	derived:openfda.package_ndc
rxcui		247835	openfda.rxcui
spl id		36a95f34-15a5-4a79-ad9d-c7ec35968bb0	id
spl set id		f30e801c-d7ae-4a6f-830b-31d86c4f5b8c	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, heat, sparts and sources of static discharge. Do not use In eyes When using this product If in eyes, rinse promptly and thoroughly with water Discontinue use if irritation and redness develop Stop use and ask doctor if Skin irritation or redness 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.