BETASEPT

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: BETASEPT
Generic name: ANTISEPTIC SURGICAL SCRUB
Manufacturer: Xttrium Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 4a6451d7-b347-37ac-e054-00144ff8d46c
SPL ID: 34007201-2d77-96fd-e063-6394a90a6327
Version: 7
Effective date: 2025-04-30
Source export date: 2026-11-06
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/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:14:48

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	NDA	019125	derived:openfda.application_number
application number		NDA019125	openfda.application_number
brand name		BETASEPT	openfda.brand_name
generic name		ANTISEPTIC SURGICAL SCRUB	openfda.generic_name
manufacturer name		Xttrium Laboratories, Inc.	openfda.manufacturer_name
ndc	package	0116-0200-04	openfda.package_ndc
ndc	package	0116-0200-01	openfda.package_ndc
ndc	package	0116-0200-32	openfda.package_ndc
ndc	package	0116-0200-08	openfda.package_ndc
ndc	package	0116-0200-16	openfda.package_ndc
ndc	package	0116-0200-30	openfda.package_ndc
ndc	product	0116-0200	openfda.product_ndc
ndc11	package	00116020001	derived:openfda.package_ndc
ndc11	package	00116020030	derived:openfda.package_ndc
ndc11	package	00116020008	derived:openfda.package_ndc
ndc11	package	00116020032	derived:openfda.package_ndc
ndc11	package	00116020004	derived:openfda.package_ndc
ndc11	package	00116020016	derived:openfda.package_ndc
rxcui		834150	openfda.rxcui
rxcui		211365	openfda.rxcui
spl id		34007201-2d77-96fd-e063-6394a90a6327	id
spl set id		4a6451d7-b347-37ac-e054-00144ff8d46c	set_id
unii		MOR84MUD8E	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 Warnings For external use only Allergy alert: This product may cause a severe allergic reaction. Symptoms may include: wheezing/difficulty breathing shock facial swelling hives rash If an allergic reaction, stop use and seek medical help right away.

Reported adverse events (FAERS/openFDA)#

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