Ultra Blue Antibacterial Foaming Skin Cleanser

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: Ultra Blue Antibacterial Foaming Skin Cleanser
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Betco Corporation, Ltd
Product type: HUMAN OTC DRUG
SPL set ID: aa8f5b05-882d-d05a-e053-2995a90abaea
SPL ID: 5b10d7b3-1a3e-60bf-e063-6294a90a1b89
Version: 7
Effective date: 2026-09-09
Source export date: 2026-10-30
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:36:21

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Ultra Blue Antibacterial Foaming Skin Cleanser	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Betco Corporation, Ltd	openfda.manufacturer_name
ndc	package	65601-759-04	openfda.package_ndc
ndc	package	65601-759-29	openfda.package_ndc
ndc	package	65601-759-57	openfda.package_ndc
ndc	product	65601-759	openfda.product_ndc
ndc11	package	65601075904	derived:openfda.package_ndc
ndc11	package	65601075957	derived:openfda.package_ndc
ndc11	package	65601075929	derived:openfda.package_ndc
rxcui		1046593	openfda.rxcui
spl id		5b10d7b3-1a3e-60bf-e063-6294a90a1b89	id
spl set id		aa8f5b05-882d-d05a-e053-2995a90abaea	set_id
unii		F5UM2KM3W7	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. Do not ingest. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation and redness develop. If irritation persists for more than 72 hours, consult a physician. KEEP OUT OF REACH OF CHILDREN . If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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