REMEDY Pain Relief Cooling Menthol Roll-ON

Manufacturer
RENU LABORATORIES, INC.
Effective date
2021-05-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:44:58

Label at a glance#

ProductREMEDY Pain Relief Cooling Menthol Roll-ON
Active ingredientMENTHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Menthol 5 percent

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

Uses for temporary relief of minor aches and pains of muscles and joints associated with

  • bruises
  • sprains
  • arthritis
  • strains

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product

Do not bandage tightly

  • avoid contact with eyes
  • do not apply to wounds or damaged skin
  • do not use with heating pads or other heating devices.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • adults and children 12 years of age and older, apply to affected area no more than 10 times a day as needed for pain
  • children under 12 years of age: do not use, consult a doctor.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Arnica Montana (Arnica) Extract, Cannabidiol (CBD) Hemp-derived, Cannabigerol (CBG) Hemp-derived, Cannabis Sativa (Hemp) Seed Oil with a proprietary mix of terpenes (alpha-bisabolol, alpha-humulene, alpha-pinene, alpha-terpinene, beta-caryophyllene, beta-myrcene, beta-pinene, caryophyllene oxide, cis-beta-ocimene, D-limonene, eucalyptol, gamma-terpinene, guaiol, linalool, menthol, p-cymene, terpinolene, trans-nerolidol), Deionized Water, Fragrance, Hydroxyethyl Cellulose, Isopropyl Alcohol, Magnesium Chloride, Mentha piperita (Peppermint) Leaf Oil, Polysorbate 80, Potassium Sorbate, Sodium Benzoate.

OTC - QUESTIONS SECTION

Questions? Comments?

contact us at

remedycbdcbg.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box artBox artREMEDY roll on labelREMEDY roll on label

Products#

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DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-61576348-615-03, 76348-615-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 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
e778b553-5d4f-49e3-e053-2995a90ae750c1fbdcea-9893-dd6c-e053-2a95a90ac4802022-08-30WarningsExact identifier
spl set id: c1fbdcea-9893-dd6c-e053-2a95a90ac480

Reported adverse events (FAERS/openFDA)#

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