Simi-Tree Natural Pain Relief

Manufacturer
Higgins and Phillips Innovations Inc.
Effective date
2020-07-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:25

Label at a glance#

ProductSimi-Tree Natural Pain Relief
Active ingredientMENTHOL
Label structure11 sections

Dosage and administration

DIRECTIONS FOR USE: Adults, adolescents, and children ≥ 2 years: Apply 1 to 4 pumps evenly to targeted area(s) up to 4 times per day

Storage and handling

Store in airtight, light-resistant container at room temperature;

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Menthol 3% w/w. Purpose: Counter Irritant; Temporarily relieves aches and pains of muscles and joints associated with arthritis, backache, strains and sprains.

Purpose

OTC - PURPOSE SECTION

Counter Irritant; Temporarily relieves aches and pains of muscles and joints associated with arthritis, backache, strains and sprains.

Direction For Use

INDICATIONS & USAGE SECTION

DIRECTIONS FOR USE: Adults, adolescents, and children ≥ 2 years: Apply 1 to 4 pumps evenly to targeted area(s) up to 4 times per day; For children (2 - 12 years) applications should be supervised by an adult.

Warnings

WARNINGS SECTION

For external use only; Avoid contact with eyes and mucous membranes;

DURATION OF USE: Consult a health care practitioner for use beyond 7 days. CAUTIONS AND WARNINGS: Call a Poison Control Center immediately if overdose or accidental ingestion occurs; Store in airtight, light-resistant container at room temperature; Stop use and consult a health care practitioner if symptoms worsen, re-occur within a few days; KNOWN ADVERSE REACTIONS: If you experience pain, swelling or blistering, stop use and get medical help right away; Stop use if hypersensitivity/allergy, rashes and/or burning discomfort occur.

Do not use

OTC - DO NOT USE SECTION

Do not apply to wounds or damaged skin; Do not tightly bandage; Do not apply with external heat, such as an electric heating pad, as this may result in excessive skin irritation or skin burn. Safety sealed for your protection, do not use if seal is broken or missing

Known Adverse Reactions

OTC - STOP USE SECTION

KNOWN ADVERSE REACTIONS: If you experience pain, swelling or blistering, stop use and get medical help right away; Stop use if hypersensitivity/allergy, rashes and/or burning discomfort occur

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.

Directions For Use

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS FOR USE: Adults, adolescents, and children ≥ 2 years: Apply 1 to 4 pumps evenly to targeted area(s) up to 4 times per day

Other information

STORAGE AND HANDLING SECTION

Store in airtight, light-resistant container at room temperature;

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Boswellia serrata (Frankincense) Essential Oil, Cetyl Alcohol, Cinnamomum zeylanicum (Ceylon Cinnamon) Bark Essential Oil, dl-Alpha-Tocopheryl Succinate, Ethylhexylglycerin, Eucalyptus polybractea (Eucalyptus) Essential Oil, Eugenia caryophyllus (Clove) Bud Essential Oil, Glycerin, Glyceryl Stearate, Grape Seed Oil, Hydroxylated Lecithin, Juniperus communis (Juniper) Fruit Essential Oil, Lavandula angustifolia (Lavender) Essential Oil, Magnesium Aluminum Silicate, Myristica fragrans (Nutmeg) Kernel Essential Oil, Oenothera biennis (Evening Primrose) Oil, Oleic Acid, Olive Oil, PEG-100 Stearate, Phenoxyethanol, Purified water, Rosmarinus officinalis (Rosemary) Leaf Essential Oil, Stearic Acid, Trolamine, Wheat Germ Oil, Xanthan Gum, Zingiber officinale (Ginger) Root Oil

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel50 g NDC: 73807-001-50

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73807-00173807-001-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
bf00fcd0-61ed-3cc3-e053-2a95a90a8e0aaa7cf451-f7c3-5d01-e053-2a95a90a9a392021-04-02WarningsExact identifier
spl set id: aa7cf451-f7c3-5d01-e053-2a95a90a9a39

Reported adverse events (FAERS/openFDA)#

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