SAN X E3

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: SAN X E3
Generic name: ALCOHOL
Manufacturer: Amerisan, LLC
Product type: HUMAN OTC DRUG
SPL set ID: d6e219a6-f4d6-b8df-e053-2995a90a5803
SPL ID: 2966b03e-d801-11bf-e063-6394a90aa169
Version: 3
Effective date: 2024-12-16
Source export date: 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:57:42

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		505G(a)(3)	openfda.application_number
brand name		SAN X E3	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Amerisan, LLC	openfda.manufacturer_name
ndc	package	69884-700-05	openfda.package_ndc
ndc	product	69884-700	openfda.product_ndc
ndc11	package	69884070005	derived:openfda.package_ndc
rxcui		1041882	openfda.rxcui
spl id		2966b03e-d801-11bf-e063-6394a90aa169	id
spl set id		d6e219a6-f4d6-b8df-e053-2995a90a5803	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 When using this product do not use in or near eyes use in a well-ventilated area Stop use and consult a doctor if irritation or redness develop. Keep out of reach of children. If swallowed, seek medical attention or contact Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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