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: Atlantis Consumer Healthcare, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 7e64e7bf-e88f-4056-c9e1-b49a277daa6c
SPL ID: 872a571c-88d2-45f9-ae87-5b0b3c900939
Version: 13
Effective date: 2025-12-24
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:45:28

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		Atlantis Consumer Healthcare, Inc.	openfda.manufacturer_name
ndc	package	67618-200-30	openfda.package_ndc
ndc	package	67618-200-04	openfda.package_ndc
ndc	package	67618-200-08	openfda.package_ndc
ndc	package	67618-200-32	openfda.package_ndc
ndc	package	67618-200-01	openfda.package_ndc
ndc	package	67618-200-16	openfda.package_ndc
ndc	product	67618-200	openfda.product_ndc
ndc11	package	67618020030	derived:openfda.package_ndc
ndc11	package	67618020032	derived:openfda.package_ndc
ndc11	package	67618020008	derived:openfda.package_ndc
ndc11	package	67618020004	derived:openfda.package_ndc
ndc11	package	67618020001	derived:openfda.package_ndc
ndc11	package	67618020016	derived:openfda.package_ndc
rxcui		834150	openfda.rxcui
rxcui		211365	openfda.rxcui
spl id		872a571c-88d2-45f9-ae87-5b0b3c900939	id
spl set id		7e64e7bf-e88f-4056-c9e1-b49a277daa6c	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 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 occurs, stop use and seek medical help right away.

Reported adverse events (FAERS/openFDA)#

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