DR GREENES GOOD STUFF PAIN RELIEF ROLL ON

Manufacturer
Sola Pharmaceuticals
Effective date
2020-05-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:28:39

Label at a glance#

ProductDR GREENES GOOD STUFF PAIN RELIEF ROLL ON
Active ingredientMENTHOL
Label structure10 sections

Dosage and administration

-Adults and children two-years of age or older. Apply to affected area not more than three to four times daily. -Children under two-years of age consuly a physician.

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 3.00%

INDICATIONS & USAGE SECTION

Topical Analgesic

Indications

OTC - PURPOSE SECTION

For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises, and strains.

Warnings

WARNINGS SECTION

-For external use only.

-Avoid contact with eyes.

-If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

-If swallowed, consult physician.

-Do not apply to wounds or damaged skin.

-Do not bandage tightly.

If pregnant or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

contact physician prior to use.

Directions

DOSAGE & ADMINISTRATION SECTION

-Adults and children two-years of age or older. Apply to affected area not more than three to four times daily.

-Children under two-years of age consuly a physician.

Storage

STORAGE AND HANDLING SECTION

Store at room temperature.

Other Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montant Flower Extract, Boswellia Serrata Extract, Camellia Sinensis (Green Tea) Extract, Cannabis Sativa (Full Spectrum Hemp) Oil, Caprylyl Glycol. Cetearyl Olivate, Cetyl Alcohol. Citric Acid, Glucosamine Sulfate, Glycerin, Glyceryl Stearate, Helianthus Annus (Sunflower) Oil, Isopropyl Alcohol, Isopropyl Myristate, Methylsufonylmethane (MSM), Phenoxyethanol, Sorbitan Olivate, Stearic Acid, Xanthan Gum.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label imageLabel image

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70512-20070512-200-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
ef1d2f22-c78b-d241-e053-2a95a90a243fa6b7dc1d-caa9-7e4f-e053-2995a90a0c442022-12-05WarningsExact identifier
spl set id: a6b7dc1d-caa9-7e4f-e053-2995a90a0c44

Reported adverse events (FAERS/openFDA)#

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