Blue Green Foam

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: Blue Green Foam
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: H2Ocean, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 8627bf8b-2cce-45de-b37f-8478462645fa
SPL ID: fe1acb32-d100-4a47-b75d-1036c0d433ff
Version: 6
Effective date: 2024-10-23
Source export date: 2026-10-30
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:21:50

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Blue Green Foam	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		H2Ocean, LLC	openfda.manufacturer_name
ndc	package	70411-100-09	openfda.package_ndc
ndc	package	70411-100-08	openfda.package_ndc
ndc	package	70411-100-07	openfda.package_ndc
ndc	package	70411-100-50	openfda.package_ndc
ndc	product	70411-100	openfda.product_ndc
ndc11	package	70411010050	derived:openfda.package_ndc
ndc11	package	70411010008	derived:openfda.package_ndc
ndc11	package	70411010007	derived:openfda.package_ndc
ndc11	package	70411010009	derived:openfda.package_ndc
rxcui		1020365	openfda.rxcui
spl id		fe1acb32-d100-4a47-b75d-1036c0d433ff	id
spl set id		8627bf8b-2cce-45de-b37f-8478462645fa	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 use • in the eyes or apply over large areas of the body • longer than 1 week unless directed by a doctor Ask a doctor before use if you have • deep or puncture wounds • animal bites • serious burns Stop use and ask a doctor if the condition persists or gets worse 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.