CareTouch

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: CareTouch
Generic name: ETHYL ALCOHOL
Manufacturer: Future Diagnostics Llc
Product type: HUMAN OTC DRUG
SPL set ID: 45f6a1da-f0ab-4783-a211-7fba5dc0530e
SPL ID: 41d33a5a-50d2-7711-e063-6294a90ac7be
Version: 10
Effective date: 2025-10-23
Source export date: 2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:38:23

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		M003	openfda.application_number
brand name		CareTouch	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		Future Diagnostics Llc	openfda.manufacturer_name
ndc	package	70393-415-22	openfda.package_ndc
ndc	package	70393-415-21	openfda.package_ndc
ndc	package	70393-415-30	openfda.package_ndc
ndc	package	70393-415-11	openfda.package_ndc
ndc	package	70393-415-01	openfda.package_ndc
ndc	product	70393-415	openfda.product_ndc
ndc11	package	70393041522	derived:openfda.package_ndc
ndc11	package	70393041530	derived:openfda.package_ndc
ndc11	package	70393041511	derived:openfda.package_ndc
ndc11	package	70393041501	derived:openfda.package_ndc
ndc11	package	70393041521	derived:openfda.package_ndc
rxcui		1041780	openfda.rxcui
spl id		41d33a5a-50d2-7711-e063-6294a90ac7be	id
spl set id		45f6a1da-f0ab-4783-a211-7fba5dc0530e	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 ■ Flammable. Keep away from fire or flame. ■ For external use only. When using this product ■ Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. ■ Discontinue use and ask a doctor if irritation or rash appears and lasts.

Reported adverse events (FAERS/openFDA)#

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