DRUG FACTS Analgesic Topical Gel

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 02:37:18

Label at a glance#

ProductUltimate Pain Block Professional Strength
Active ingredientNAJA NAJA VENOM
Label structure9 sections

Indications and uses

Temporarily relieves joint pain associated with overuse and pain associated with arthritis.

Dosage and administration

Remove protective wrapping. Liberally apply gel to the affected area and rub into joints. Use 3-4 times per day for the first week. Use as needed thereafter to relieve discomfort. Allow several days for drug to take maximum effect.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Asian Cobra Venom 4X

Purpose

OTC - PURPOSE SECTION

Analgesic*

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Benzalkonium chloride, Ethanol, Methocel, Propylene glycol, Saline

Uses:

INDICATIONS & USAGE SECTION

Temporarily relieves joint pain associated with overuse and pain associated with arthritis.

Warnings:

WARNINGS SECTION

  • 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.

Directions For Use:

DOSAGE & ADMINISTRATION SECTION

  • Remove protective wrapping.
  • Liberally apply gel to the affected area and rub into joints.
  • Use 3-4 times per day for the first week. Use as needed thereafter to relieve discomfort.
  • Allow several days for drug to take maximum effect.

Other Information:

OTHER SAFETY INFORMATION

OTC - DO NOT USE SECTION

  • Do not use if container seal is broken prior to opening.
  • This product is intended for use in cases of recurring joint pain.
  • This product is NOT intended to treat disease, it provides a temporary level of comfort, relief and a feeling of wellness.
  • This product has been determined to be safe and effective for moderate to severe (Stage 2) chronic pain, as indicated by the Homeopathic Pharmacopeia of the United States.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Questions?

OTC - QUESTIONS SECTION

1-888-381-HEALTH

Principal Display Panel - 8 oz Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PHYSICIAN'S
TOTAL HEALTH

ULTIMATE
PAIN BLOCK

PROFESSIONAL STRENGTH

CLINICALLY PROVEN LONG-LASTING
PAIN & INFLAMMATION RELIEF

Joint Pain • Neck Pain
Arthritis Pain • Neuropathic Pain
Pain from Repetitive Stress

TOPICAL GEL

HOMEOPATHIC

8OZ. NET WT.

Principal Display Panel - 8 oz Bottle Label
Principal Display Panel - 8 oz Bottle Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47219-315-08Ultimate Pain Block Professional Strength1 in 1 BOXGEL12
47219-315-08Ultimate Pain Block Professional Strength235 mL in 1 BOTTLE, DISPENSINGGEL2352

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47219-31547219-315-08

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ultimate Pain Block Professional StrengthNAJA NAJA VENOMNutra Pharma Corporation5af2ef6d-3450-41f4-88c7-0d8a68fa9bfa2025-11-04WarningsExact identifier
ndc (package): 47219-315-08
ndc (product): 47219-315
ndc11 (package): 47219031508
spl id: 42c78db7-a105-dd6f-e063-6394a90abdca
spl set id: 5af2ef6d-3450-41f4-88c7-0d8a68fa9bfa

Reported adverse events (FAERS/openFDA)#

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