Plus Relief

Manufacturer: Nutra Pharma Corporation
Effective date: 2025-11-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:37:17

Label at a glance#

ProductPlus Relief

Active ingredientNAJA NAJA VENOM

Label structure7 sections

Dosage and administration

Remove protective wrapping. Liberally apply gel to affected area. Rub thoroughly into hands and joints.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Asian Cobra Venom 6X

PURPOSE

OTC - PURPOSE SECTION

Analgesic*

*Claims based on traditional Homeopathic practice not accepted medical evidence. Not FDA accepted.

Directions:

DOSAGE & ADMINISTRATION SECTION

Remove protective wrapping.
Liberally apply gel to affected area.
Rub thoroughly into hands and joints.

INDICATIONS & USAGE SECTION

USE 3-4 TIMES A DAY.

Note:It may take several days to induce relief. Use within 90 days of opening. Store at 50° to 80°F.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Benzalkonium Chloride, Ethanol, Methocel, Propylene glycol, Saline.

NDC 47219-312-02■ HOMEOPATHIC

WARNINGS:

WARNINGS SECTION

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.

PREGNANCY SECTION

Pregnant or nursing women and children should consult a physician before use.

OTC - DO NOT USE SECTION

Do not use if seal is broken prior to opening.

This product is NOT intended to treat disease. It provides a temporary level of comfort, relief and a feeling of wellness.

Principal Display Panel - 2 oz Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AVINIHEALTH ™
ADVANCES IN NATURAL HEALING

PLUS
RELIEF

Chronic Pain Relief

SUPER STRENGTH

ROLL-ON APPLICATOR

Joint Pain ■ Neck Pain ■ Arthritis Pain
Pain from Repetitive Stress

2 oz. net wt.

Principal Display Panel - 2 oz Bottle Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
47219-312-02	Plus Relief	60 mL in 1 BOTTLE, DISPENSING	GEL	60		2
47219-312-02	Plus Relief	1 in 1 BOX	GEL	1		2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Plus Relief
NAJA NAJA VENOM
BENZALKONIUM CHLORIDE
ALCOHOL
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
PROPYLENE GLYCOL
ISOTONIC SODIUM CHLORIDE SOLUTION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
47219-312	47219-312-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	IACT
ALCOHOL	3K9958V90M	IACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED	K679OBS311	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ISOTONIC SODIUM CHLORIDE SOLUTION	VR5Y7PDT5W	IACT
NAJA NAJA VENOM	ZZ4AG7L7VM	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Plus Relief	NAJA NAJA VENOM	Nutra Pharma Corporation	4595e797-befe-42a8-a56a-2a1a2a1e4a29	2025-11-04	Warnings	Exact identifier ndc (package): 47219-312-02 ndc (product): 47219-312 ndc11 (package): 47219031202 spl id: 42c61015-141a-054e-e063-6394a90ab255 spl set id: 4595e797-befe-42a8-a56a-2a1a2a1e4a29

Reported adverse events (FAERS/openFDA)#

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