Nozin Nasal Sanitizer (Antiseptic)

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: Nozin Nasal Sanitizer (Antiseptic)
Generic name: ALCOHOL
Manufacturer: Global Life Technologies Corp.
Product type: HUMAN OTC DRUG
SPL set ID: c670ac11-0656-4d85-868e-3a407c9952a3
SPL ID: d320435c-e55b-4d0f-8ee7-66e612790a58
Version: 6
Effective date: 2025-05-05
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:19:14

Harmonized routes table
Harmonized routes
NASAL

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Nozin Nasal Sanitizer (Antiseptic)	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Global Life Technologies Corp.	openfda.manufacturer_name
ndc	package	82539-211-50	openfda.package_ndc
ndc	package	82539-211-12	openfda.package_ndc
ndc	package	82539-211-11	openfda.package_ndc
ndc	package	82539-211-02	openfda.package_ndc
ndc	package	82539-211-10	openfda.package_ndc
ndc	product	82539-211	openfda.product_ndc
ndc11	package	82539021112	derived:openfda.package_ndc
ndc11	package	82539021110	derived:openfda.package_ndc
ndc11	package	82539021111	derived:openfda.package_ndc
ndc11	package	82539021102	derived:openfda.package_ndc
ndc11	package	82539021150	derived:openfda.package_ndc
spl id		d320435c-e55b-4d0f-8ee7-66e612790a58	id
spl set id		c670ac11-0656-4d85-868e-3a407c9952a3	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. Do not use in the eyes on mucous membranes if you have history of nasal bleeding or irritation if you have allergies to any of the ingredients Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours 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.