HAND SANITIZER SANDALWOOD WAVES

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: HAND SANITIZER SANDALWOOD WAVES
Generic name: ALCOHOL
Manufacturer: SCENT THEORY PRODUCTS LLC
Product type: HUMAN OTC DRUG
SPL set ID: 24893800-464a-16ca-e063-6294a90a9065
SPL ID: 249c00c1-44c6-af77-e063-6394a90a122b
Version: 2
Effective date: 2024-10-16
Source export date: 2026-10-12
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:44:03

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		HAND SANITIZER SANDALWOOD WAVES	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		SCENT THEORY PRODUCTS LLC	openfda.manufacturer_name
ndc	package	76891-142-11	openfda.package_ndc
ndc	product	76891-142	openfda.product_ndc
ndc11	package	76891014211	derived:openfda.package_ndc
rxcui		1020364	openfda.rxcui
spl id		249c00c1-44c6-af77-e063-6394a90a122b	id
spl set id		24893800-464a-16ca-e063-6294a90a9065	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: HANDS FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME. WHEN USING THIS PRODUCT KEEP OUT OF EYES. IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN. DO NOT INHALE OR INGEST. STOP USE AND ASK A DOCTOR IF IRRITATION AND REDNESS DEVELOP CONDITION PERSISTS FOR MORE THAN 72 HOURS

Reported adverse events (FAERS/openFDA)#

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