DR GREENES GOOD STUFF PAIN RELIEF ROLL ON- menthol liquid liquid

DR GREENES GOOD STUFF PAIN RELIEF ROLL ON by

Drug Labeling and Warnings

DR GREENES GOOD STUFF PAIN RELIEF ROLL ON by is a Otc medication manufactured, distributed, or labeled by Sola Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Menthol 3.00%

INDICATIONS & USAGE

Topical Analgesic

Indications

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

Warnings

-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

-If swallowed, consult physician.

-Do not apply to wounds or damaged skin.

-Do not bandage tightly.

If pregnant or breast feeding

contact physician prior to use.

Directions

-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

Store at room temperature.

Other Ingredients

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:

INGREDIENTS AND APPEARANCE

DR GREENES GOOD STUFF PAIN RELIEF ROLL ON 
menthol liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70512-200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
STEARIC ACID (UNII: 4ELV7Z65AP)
XANTHAN GUM (UNII: TTV12P4NEE)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
WATER (UNII: 059QF0KO0R)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
SORBITAN OLIVATE (UNII: MDL271E3GR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70512-200-90	88.7 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	05/28/2020

Labeler - Sola Pharmaceuticals (080121345)