NO PAIN MORE GAIN- menthol cream

No Pain More Gain by

Drug Labeling and Warnings

No Pain More Gain by is a Otc medication manufactured, distributed, or labeled by Lugus Group LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Menthol (0.1%)

Purpose

Topical Analgesic

PURPOSE

Use

For temporary relief of muscle and joint pain associated with arthritis, backaches, bruises, strains, sports injuries and muscle stiffness

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions

Shake Well. Adults and children of 2 years and older apply to the affected areas up to 6 times a day. Massage in gently.

WARNINGS

Warnings

For external use only Avoid contact with the eyes and mucous membranes Do not use with a heating pad Do not use on open wounds or broken skin

INDICATIONS & USAGE

100% Vegan

No Pain More Gain Cream

Moisturizing Pain Relief

NPMG is 100% vegan Gluten-free Free of paraben, paraffin and silicone oil Made from spring water Not tested on animals

For pain treatment and as preventive measure. Best for use on large areas. No Pain More Gain (NPMG) provides temporary but long lasting pain relief and moisturizes the skin. The natural alternative with the advanced German formula starts to work on contact. NPMG penetrates deeply, absorbs quickly and has a fresh and pleasant scent.

NPMG Cream is a product

Lugus Group LLC, Buffalo, WY 82834

NET WT 5.07 fl oz (150 ml)

INACTIVE INGREDIENT

Inactive Ingredients

Alcohol, Ascorbic Acid, Ascorbyl Palmitate, Benzoic Acid, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Citral, Citric Acid, Citrus Medica Limonum (Lemon) Peel Oil, Dehydroacetic Acid, Dicaprylyl Carbonate, Ethylhexylglycerin, Ethylhexyl Stearate, Galactoarabinan, Glycerin, Gold, Limonene, Panthenol, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate, Phenoxyethanol, Platinum Powder, PPG-3 Benzyl Ether Myristate, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Silica, Sodium Hydroxide, Sodium Stearoyl Glutamate, Squalene, Tetrasodium Glutamate Diacetate, Tocopherol, Water, Xanthan gum.

ASK DOCTOR

Stop use and ask a doctor if

Condition worsens Skin irritation occurs Symptoms persist for more than 7 days or clear up and occur again within a few days

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NO PAIN MORE GAIN 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69161-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
GOLD (UNII: 79Y1949PYO)
WATER (UNII: 059QF0KO0R)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
GLYCERIN (UNII: PDC6A3C0OX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
ALMOND OIL (UNII: 66YXD4DKO9)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
PPG-3 BENZYL ETHER MYRISTATE (UNII: 8075L58MKO)
PANTHENOL (UNII: WV9CM0O67Z)
SQUALANE (UNII: GW89575KF9)
XANTHAN GUM (UNII: TTV12P4NEE)
GALACTOARABINAN (UNII: SL4SX1O487)
LEMON OIL (UNII: I9GRO824LL)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TOCOPHEROL (UNII: R0ZB2556P8)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PLATINUM (UNII: 49DFR088MY)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALCOHOL (UNII: 3K9958V90M)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
CITRAL (UNII: T7EU0O9VPP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69161-001-01	100 mg in 1 PACKAGE; Type 0: Not a Combination Product	08/29/2014	05/02/2017
2	NDC: 69161-001-02	150 mg in 1 PACKAGE; Type 0: Not a Combination Product	05/02/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/29/2014

Labeler - Lugus Group LLC (079463507)

Registrant - Lugus Group LLC (079463507)

Establishment
Name	Address	ID/FEI	Business Operations
Lugus Group LLC		079463507	label(69161-001)