Nyloxin

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: Nyloxin
Generic name: NAJA NAJA VENOM
Manufacturer: Nutra Pharma Corporation
Product type: HUMAN OTC DRUG
SPL set ID: dee9027d-5245-40d4-a4ba-052a1ecfe786
SPL ID: 8f1b83c5-c49e-4c94-b03a-6bb4bcb2e48a
Version: 6
Effective date: 2025-10-14
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:46:07

Harmonized routes table
Harmonized routes
ORAL

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Nyloxin	openfda.brand_name
generic name		NAJA NAJA VENOM	openfda.generic_name
manufacturer name		Nutra Pharma Corporation	openfda.manufacturer_name
ndc	package	47219-200-01	openfda.package_ndc
ndc	product	47219-200	openfda.product_ndc
ndc11	package	47219020001	derived:openfda.package_ndc
spl id		8f1b83c5-c49e-4c94-b03a-6bb4bcb2e48a	id
spl set id		dee9027d-5245-40d4-a4ba-052a1ecfe786	set_id
unii		ZZ4AG7L7VM	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: - Side effects may include headache, nausea, sore throat, allergic rhinitis, gastrointestinal discomfort. - If symptoms persist or worsen, stop using this product and consult a physician. - When Using This Product: avoid contact with the eyes. If product gets into eyes, flush with water. Seek medical attention.

Reported adverse events (FAERS/openFDA)#

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