warnings
Warnings: - For external use only - If symptoms persist or worsen, discontinue use and seek medical attention. - Avoid contact with eyes. If product gets into eyes, flush with water. Seek medical attention. - Not for use on open wounds.
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
- Brand name
- Nyloxin
- Generic name
- NAJA NAJA VENOM
- Manufacturer
- Nutra Pharma Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c28c50db-4b6b-4307-8fcb-9020d6ae9cd3
- SPL ID
- cc0046fd-33b6-462c-bae8-8cd20d5713fb
- Version
- 5
- Effective date
- 2025-10-20
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:10
| 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.
| 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 | 47219-311-02 | openfda.package_ndc |
| ndc | product | 47219-311 | openfda.product_ndc |
| ndc11 | package | 47219031102 | derived:openfda.package_ndc |
| spl id | cc0046fd-33b6-462c-bae8-8cd20d5713fb | id | |
| spl set id | c28c50db-4b6b-4307-8fcb-9020d6ae9cd3 | set_id | |
| unii | ZZ4AG7L7VM | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.