Smart Care 3 HAND SANITIZERS 1.35 FL OZ (OCEAN, CEDAR and CYPRESS, SANDALWOOD)

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: Smart Care 3 HAND SANITIZERS 1.35 FL OZ (OCEAN, CEDAR and CYPRESS, SANDALWOOD)
Generic name: ETHYL ALCOHOL
Manufacturer: Ashtel Studios, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 83be1e12-c7a9-4e35-a813-24d05d0f9505
SPL ID: 70d591ca-32df-493f-83b2-36fd685ac97d
Version: 1
Effective date: 2025-11-22
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:52

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Smart Care 3 HAND SANITIZERS 1.35 FL OZ (OCEAN, CEDAR and CYPRESS, SANDALWOOD)	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		Ashtel Studios, Inc.	openfda.manufacturer_name
ndc	package	70108-274-01	openfda.package_ndc
ndc	package	70108-273-01	openfda.package_ndc
ndc	package	70108-266-01	openfda.package_ndc
ndc	package	70108-272-01	openfda.package_ndc
ndc	product	70108-266	openfda.product_ndc
ndc11	package	70108027401	derived:openfda.package_ndc
ndc11	package	70108026601	derived:openfda.package_ndc
ndc11	package	70108027201	derived:openfda.package_ndc
ndc11	package	70108027301	derived:openfda.package_ndc
rxcui		1041849	openfda.rxcui
spl id		70d591ca-32df-493f-83b2-36fd685ac97d	id
spl set id		83be1e12-c7a9-4e35-a813-24d05d0f9505	set_id

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 • If you are allergic to any of the ingredients. When using this product • Do not get into eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor • If irritation or rash develops and continues for more than 72 hours. Keep out of reach of children. If swallowed, call Poison Help at 1-800-222-1222 or go to PoisonHelp.org.

Reported adverse events (FAERS/openFDA)#

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