FlexaCure

Manufacturer
Symedic LLC
Effective date
2019-09-03
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:00:11

Label at a glance#

ProductThe Relief Company
Active ingredientMENTHOL
Label structure12 sections

Dosage and administration

Adults and children 12 years of age and older: Spray onto affected areas no more than 4 times daily; massage not necessary. Children under 12 years of age: consult a physician.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 2%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Use

INDICATIONS & USAGE SECTION

Temporary relief from minor aches and pains of sore muscles & joints associated with

  • arthritis
  • simple backache
  • strains
  • bruises
  • sprains.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product

  • Avoid contact with the eye or mucous membranes
  • Do not apply to wounds or damaged skin
  • Do not use with other ointments, creams, sprays or liniments
  • Do not apply to irritated skin or if excessive irritation develops
  • Do not bandage
  • Wash hands after use with cool water
  • Do not use with heating pad or device
  • Contains sulfur compounds.

OTC - STOP USE SECTION

Stop use and ask a doctor if conditions worsen, or if symptoms persist for more than 7 days, or clear up and reoccur.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If accidentally ingested, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: Spray onto affected areas no more than 4 times daily; massage not necessary. Children under 12 years of age: consult a physician.

Other Information

OTHER SAFETY INFORMATION

Store in a cool dry place with lid closed tightly.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

dimethyl sulfone, dimethyl sulfoxide, eucalyptus oil*, hydrogen peroxide, peppermint oil*, spike lavender oil*, water.

Relleve Naturals - Menthol Spray [​7140288801]

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

New

7140288801

Relleve Naturals

Deep Penetrating Pain Relief

  • All-Natural Formula
  • Essential Oil Blend
  • For Muscle & Joint Pain

Topical Spray

1 fl oz / 30 ml

Relleve Naturals LabelsRelleve Naturals Labels

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71402-101-012021-01-29C16284748780-1ba0f9c33-1e6e-a910-e053-dadaa90a0b858e60a0ef-8947-7fa7-e053-2995a90a065c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71402-101-01The Relief Company89 mL in 1 BOTTLE, WITH APPLICATORGEL895

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71402-101THE RELIEF COMPANY (MENTHOL) GEL [SYMEDIC LLC]5Legacy NDC, 1 package rows20190904_8e60a0ef-8947-7fa7-e053-2995a90a065c.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71402-10171402-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
91ab319c-db6c-7749-e053-2a95a90ae6fd8e60a0ef-8947-7fa7-e053-2995a90a065c2019-09-03WarningsExact identifier
spl id: 91ab319c-db6c-7749-e053-2a95a90ae6fd
spl set id: 8e60a0ef-8947-7fa7-e053-2995a90a065c

Reported adverse events (FAERS/openFDA)#

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