Activate Joint and Muscle Relief Cream

Manufacturer
Liberty Health Supply, LLC
Effective date
2017-11-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:10:31

Label at a glance#

ProductActivate Joint and Muscle Relief
Active ingredientLIDOCAINE HYDROCHLORIDE, MENTHOL
Label structure7 sections

Dosage and administration

Adults and children two-years of age or older: Apply small amount to affected area not more than three to four times daily. Apply after shower or bath for best result Children under two-years of age: consult a physician

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

4.00% Lidocaine HCl 
1.00% Menthol

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Indications:

INDICATIONS & USAGE SECTION

For the temporary relief of pain and itching due to minor burns, sunburn, minor cuts, scrapes, insect bites and minor skin irritations

Warnings:

WARNINGS SECTION

  • For external use only.
  • Do not use in large quantities, particularly over raw or blistered areas.
  • If symptoms persisit for more than seven days, discontinue use and consult physician.
  • Avoid contact with eyes. Rinse well if contact occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, consult physician.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Adults and children two-years of age or older: Apply small amount to affected area not more than three to four times daily.
  • Apply after shower or bath for best result
  • Children under two-years of age: consult a physician

Additional information:

SPL UNCLASSIFIED SECTION

Store at room temperature.

Other Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana (Arnica) Extract, Azadirachta Indica (Neem) Oil,  Butyrospermum Parkii (Shea) Butter, C13-14 Isoparaffin, Calophyllum Inophyllum (Tamanu) Seed Oil, Camellia Sinensis (Green Tea) Extract, Cetearyl Alcohol, Chondroitin Sulfate, Citric Acid, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Emu Oil, Ethylhexylglycerin, Glycerin,
Glyceryl Stearate, Glucosamine Sulfate, Laureth-7, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Polysorbate-20, Sesamum
Indicum (Sesame) Seed Oil, SD-Alcohol 40B, Stearic Acid, Tocopheryl Acetate (Vitamin E), Theobroma Cacao (Cocoa) Butter, Xanthan Gum.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71868-08071868-080-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 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
071db38c-3138-fb5e-e063-6394a90abf5d24b5b595-3ed9-47fc-8086-989a2a19142d2023-10-07WarningsExact identifier
spl set id: 24b5b595-3ed9-47fc-8086-989a2a19142d

Reported adverse events (FAERS/openFDA)#

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