YOU RELIEF MUSCLE AND JOINT RUB- menthol cream

You Relief Muscle and Joint Rub by

Drug Labeling and Warnings

You Relief Muscle and Joint Rub by is a Otc medication manufactured, distributed, or labeled by THE FEEL GOOD LAB, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Menthol 1.25%

Purpose

Topical pain relief

Indications

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

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: consult a physician.

Inactive ingredients

achillea millefolium (yarrow) extract, aloe barbadensis (aloe vera gel) juice, aqua (deionized water), arnica montana (arnica) extract, beeswax, bixa orellana (annatto) seed extract, boswellia serrata extract, calendula officinalis (marigold) flower extract, caprylic/capric triglyceride, cetearyl olivate, cetyl myristoleate, chondroitin sulfate, curcuma longa (turmeric) extract, dimethyl sulfone (msm), emu oil, gluconolactone, glucosamine hcl, glycerin, glyceryl stearate se, harpagophytum procumbens (devil's claw) root extract, helianthus annuus (sunflower) seed oil, ilex paraguariensis (yerba mate) leaf extract, magnesium sulfate, scutellaria baicalensis (baikal skullcap) root extract, sodium benzoate, sorbitan olivate, stearic acid, tocopheryl acetate (vitamin e), xanthan gum, yucca aloifolia extract.

Package Labeling:

INGREDIENTS AND APPEARANCE

YOU RELIEF MUSCLE AND JOINT RUB 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70554-732
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	12.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA (UNII: O80TY208ZW)
YELLOW WAX (UNII: 2ZA36H0S2V)
BIXA ORELLANA SEED (UNII: O87354RZ5A)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)
TURMERIC (UNII: 856YO1Z64F)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
EMU OIL (UNII: 344821WD61)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITAN OLIVATE (UNII: MDL271E3GR)
STEARIC ACID (UNII: 4ELV7Z65AP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70554-732-02	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/10/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	03/16/2016

Labeler - The Feel Good Lab, LLC (080160949)