warnings
WARNINGS: For external use only. If pain persists, consult a physician. Avoid contact with eyes. If product gets into eyes, flush with water. Seek medical attention. Not for use on open wounds.
Plus Relief
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
- Plus Relief
- Generic name
- NAJA NAJA VENOM
- Manufacturer
- Nutra Pharma Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5b715c5d-1f0d-4abf-b3c7-2c9052653082
- SPL ID
- 42b526c7-28cc-5aac-e063-6294a90a1eb8
- Version
- 2
- Effective date
- 2025-11-03
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:57:21
| 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 | Plus Relief | openfda.brand_name | |
| generic name | NAJA NAJA VENOM | openfda.generic_name | |
| manufacturer name | Nutra Pharma Corporation | openfda.manufacturer_name | |
| ndc | package | 47219-302-08 | openfda.package_ndc |
| ndc | product | 47219-302 | openfda.product_ndc |
| ndc11 | package | 47219030208 | derived:openfda.package_ndc |
| spl id | 42b526c7-28cc-5aac-e063-6294a90a1eb8 | id | |
| spl set id | 5b715c5d-1f0d-4abf-b3c7-2c9052653082 | 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.