FDA.reportPublic FDA data

Active ingredient

Manufacturer
Micelle Laboratories, Incorporated
Effective date
2026-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-17 21:45:47

Label at a glance#

ProductNervionix Pro Magnesium Ice
Active ingredientLIDOCAINE HYDROCHLORIDE, MENTHOL, MAGNESIUM CHLORIDE
Label structure8 sections

Indications and uses

Soothing relief of pain, stiffness, tingling, or burning nerve pain associated with arthritis, muscles and joint pains, cramps and soreness, backache, and sciatica.

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

  • Soothing relief of pain, stiffness, tingling, or burning nerve pain associated with arthritis, muscles and joint pains, cramps and soreness, backache, and sciatica.

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), FD&C Blue No. 1.

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#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87752-00387752-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE ARBORESCENS LEAF JUICE09TD8L5SQVIACT
GLYCERYL STEARATE230OU9XXE4IACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
PENTYLENE GLYCOL50C1307PZGIACT
TRIETHANOLAMINE9O3K93S3TKIACT
CETYL ALCOHOL936JST6JCNIACT
PETROLATUM4T6H12BN9UIACT
DIMETHYL ISOSORBIDESA6A6V432SIACT
PEG-100 STEARATEYD01N1999RIACT
APRICOT KERNEL OIL54JB35T06AIACT
GRAPE SEED OIL930MLC8XGGIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
ALPHA LIPOIC ACID73Y7P0K73YIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
FRAGRANCE LAVENDER ORC18009791B40MIN2W5IACT
FD&C BLUE NO. 1H3R47K3TBDIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
MENTHOLL7T10EIP3AACTIB
MAGNESIUM CHLORIDE02F3473H9OACTIM

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
Nervionix Pro Magnesium IceLIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDEMicelle Laboratories, Incorporatedc11e0963-90fb-48c6-938a-3dcbbad17aca2026-07-09WarningsExact identifier
ndc (package): 87752-003-01
ndc (product): 87752-003
ndc11 (package): 87752000301
spl id: 5631a520-7225-b6c8-e063-6294a90a1a87
spl set id: c11e0963-90fb-48c6-938a-3dcbbad17aca

Reported adverse events (FAERS/openFDA)#

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