Active ingredient

Manufacturer
Micelle Laboratories, Incorporated
Effective date
2026-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-07-17 21:35:45

Label at a glance#

ProductNervionoix Pro Neuropathy Fast Acting Cream
Active ingredientLIDOCAINE HYDROCHLORIDE, MENTHOL, MAGNESIUM CHLORIDE
Label structure8 sections

Indications and uses

Temporarily relieves minor pain associated with • neuropathy, nerve discomfort, arthritis, simple backache, muscle strains, sprains, bruises, or cramps.

Dosage and administration

Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: Consult a doctor before use. We recommend testing a small amount of cream on your skin first to check for skin reaction and comfort level; wait 15 minutes before applying to affected area if you are happy with the comfort level.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 3.7%
Lidocaine HCL  1.0%
Magnesium Chloride  2.0%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic Cream

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain associated with • neuropathy, nerve discomfort, arthritis, simple backache, muscle strains, sprains, bruises, or cramps.

Warnings

WARNINGS SECTION

For external use only

Do not use

  • On damaged or broken skin.

When using this product

  • Avoid contact with the eyes.
  • Do not bandage tightly.

Stop use and ask a doctor if

Rash or irritation develops and lasts.
Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily.
  • Children under 12 years of age: Consult a doctor before use.
  • We recommend testing a small amount of cream on your skin first to check for skin reaction and comfort level; wait 15 minutes before applying to affected area if you are happy with the comfort level.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Aloe Arborescens Leaf Juice (Fillet), Glyceryl Stearate, Caprylic/Capric Triglyceride,Pentylene Glycol, Triethanolamine, Cetyl Alcohol, Petrolatum, Dimethyl Isosorbide, PEG-100 Stearate, Prunus Armeniaca (Apricot) Kernel Oil, Vitis Vinifera (Grape) Seed Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Alpha Lipoic Acid, Ethylhexylglycerin and Phenoxyethanol, PEG-7 Glyceryl Cocoate, Fragrance (Lavender)

Other information

SPL UNCLASSIFIED SECTION

Protect the product in this container from excessive heat and direct sun.

Questions? Need Help? Support@NerveGuardRelief.com

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87752-00287752-002-01, 87752-002-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
Nervionoix Pro Neuropathy Fast Acting CreamLIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDEMicelle Laboratories, Incorporated23abdf62-03a8-4aaa-8e29-0e2585b5ade72026-06-24WarningsExact identifier
ndc (package): 87752-002-02
ndc (package): 87752-002-01
ndc (product): 87752-002
ndc11 (package): 87752000201
ndc11 (package): 87752000202
spl id: 54ff1148-4d74-f752-e063-6394a90a206a
spl set id: 23abdf62-03a8-4aaa-8e29-0e2585b5ade7

Reported adverse events (FAERS/openFDA)#

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