NERVE PAIN FORMULA

Manufacturer
PROTEGE' MEDIA LLC
Effective date
2021-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:05

Label at a glance#

ProductNERVE PAIN FORMULA
Active ingredientNAJA NAJA VENOM, CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP, AGKISTRODON PISCIVORUS VENOM
Label structure8 sections

Dosage and administration

• Do not use if tamper proof cover is missing. • Use graduated dropper to take 0.5 ml of liquid. • Put the liquid directly into the mouth or under the tongue. • Start using twice per day. Use as needed thereafter to relieve discomfort. • Allow several days for product to take maximum effect. • Use within 60 days of opening. Store at 50° to 75°F (10°C to 24°C).

Label contents#

Full prescribing information#

Active Ingredients                                                                                  Purpose

OTC - ACTIVE INGREDIENT SECTION

Cobra venom (Naja naja) 4X (0.1mg) HPUS                                       Analgesic
Hemp extract (Cannabis sativa) 2X (16.95mg) HPUS                              Anti-inflammatory
Mocassin venom (A.piscivorus) 6X (0.001mg) HPUS                            Analgesic

Approximately 56 doses per container

Reference: the Homeopathic Pharmacopoeia of the United States (HPUS)

Indication:

INDICATIONS & USAGE SECTION

Temporarily relieves pain associated with neuropathy, periodic neuralgia, neck and back pain.

Warnings:

WARNINGS SECTION

  • Side effects might include headache, nausea, sore throat, allergic rhinitis, gastrointestinal discomfort, itchiness or mild rash.
  • If symptoms persist or worsen, stop using this product and consult a physician.
  • Avoid contact with eyes. If product gets into eyes, flush with water, seek medical attention.
  • If pregnant or breastfeeding, ask a health professional before use.
  • If diagnosed with psychiatric or mood disorder, seek medical advice before use.
  • Keep out of reach of children.

Directions For Use:

DOSAGE & ADMINISTRATION SECTION

• Do not use if tamper proof cover is missing.
• Use graduated dropper to take 0.5 ml of liquid.
• Put the liquid directly into the mouth or under the tongue.
• Start using twice per day. Use as needed thereafter to relieve discomfort.
• Allow several days for product to take maximum effect.
• Use within 60 days of opening. Store at 50° to 75°F (10°C to 24°C).

Other Information:

SPL UNCLASSIFIED SECTION

  • Consult a medical professional if using other medications for known interactions.
  • Cannabidiol in hemp extract may alter the metabolism of other drugs.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Citric acid, flavoring, glycerin, potassium sorbate, purified water, sodium benzoate, vitamin C, xanthan gum.

Comments, Questions or Complaints?

OTC - QUESTIONS SECTION

Call 888-735-4009 or info@promedxnow.com.

PRODUCT LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76524-231-012021-07-23C16284748780-1c7ccaba7-23fa-fd44-e053-dadaa90aa01bDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76524-231-01NERVE PAIN FORMULA28 mL in 1 BOTTLE, DROPPERLIQUID281

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76524-231NERVE PAIN FORMULA (COBRA VENOM (NAJA NAJA) 4X, HEMP EXTRACT (CANNABIS SATIVA) 2X, MOCCASIN VENOM (A.PISCIVORUS) 6X) LIQUID [PROTEGE' MEDIA LLC]1Legacy NDC, 1 package rows20210109_b8691c99-eb91-3305-e053-2995a90a9488.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76524-23176524-231-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
b8689d00-25c5-535d-e053-2a95a90a30aeb8691c99-eb91-3305-e053-2995a90a94882021-01-08WarningsExact identifier
spl id: b8689d00-25c5-535d-e053-2a95a90a30ae
spl set id: b8691c99-eb91-3305-e053-2995a90a9488

Reported adverse events (FAERS/openFDA)#

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