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#

ProductNuturna Sciatica
Active ingredientMENTHOL
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%

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

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Arnica Montana Flower Extract, Carbomer, Ilex Paraguariensis (Yerba Mate) Extract, Isopropyl Alcohol, Melaleuca Alternifolia (Tea Tree) Oil, Phenoxyethanol, Methylsulfonylmethane (MSM), EDTA, Polysorbate-20, Pyridoxine HCl (Vitamin B6), Tocopheryl Acetate (Vitamin E), DI Water, Triethanolamine, FD & C Blue #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#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87752-00587752-005-01, 87752-005-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
Nuturna SciaticaMENTHOLMicelle Laboratories, Incorporatedff200864-bedf-4138-bdec-2b23701406dd2026-07-09WarningsExact identifier
ndc (package): 87752-005-02
ndc (package): 87752-005-01
ndc (product): 87752-005
ndc11 (package): 87752000501
ndc11 (package): 87752000502
spl id: 56319f55-54d7-ba49-e063-6294a90acde5
spl set id: ff200864-bedf-4138-bdec-2b23701406dd

Reported adverse events (FAERS/openFDA)#

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