Plus Relief

Manufacturer: Nutra Pharma Corporation
Effective date: 2025-11-03
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 structure8 sections

Dosage and administration

Remove clear cap. Open mouth. Press pump top down 2 times directly into mouth or under your tongue. Use spray initially every 3-4 hours. Note: It may take several days to induce relief. Use within 90 days of opening. Store at 50° to 80°F.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Analgesic*

PURPOSE

OTC - PURPOSE SECTION

Asian Cobra Venom 6X

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

INDICATIONS & USAGE SECTION

ORAL SPRAY-HOMEOPATHIC

Directions:

DOSAGE & ADMINISTRATION SECTION

Remove clear cap.

Open mouth. Press pump top down 2 times directly into mouth or under your tongue. Use spray initially every 3-4 hours.

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

KEEP OUT OF THE REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

NDC 47219-211-01

WARNINGS:

WARNINGS SECTION

For oral use only.
If pain persists, consult a physician.
Overuse may induce headaches.
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.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Flavoring, Purified Water, Sodium benzoate, sodium phosphate, Xylitol.

Principal Display Panel - 1 oz Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AVINIHEALTH ™
ADVANCES IN NATURAL HEALING

PLUS
RELIEF

Chronic Pain Relief

SUPER STRENGTH

Back Pain-Neck Pain-Joint Pain
Headaches ■ Migraines ■ Neuralgia

1 oz. net wt.

Principal Display Panel - 1 oz Bottle Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
47219-211-01	Plus Relief	30 mL in 1 BOTTLE, SPRAY	SPRAY, METERED	30		2
47219-211-01	Plus Relief	1 in 1 BOX	SPRAY, METERED	1		2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Plus Relief
NAJA NAJA VENOM
WATER
SODIUM BENZOATE
SODIUM PHOSPHATE
XYLITOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
47219-211	47219-211-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
SODIUM PHOSPHATE	SE337SVY37	IACT
XYLITOL	VCQ006KQ1E	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	57d9bcb8-7bc0-402c-b181-d151c8b45cd3	2025-11-03	Warnings	Exact identifier ndc (package): 47219-211-01 ndc (product): 47219-211 ndc11 (package): 47219021101 spl id: 42b43f61-e954-69fb-e063-6394a90a7f73 spl set id: 57d9bcb8-7bc0-402c-b181-d151c8b45cd3

Reported adverse events (FAERS/openFDA)#

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