NO PAIN MORE GAIN- menthol cream 
Lugus Group LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient

Menthol (0.1%)

Purpose

Topical Analgesic

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.

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

• 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

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 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.

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

NPMG Cream

NO PAIN MORE GAIN 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69161-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69161-001-01100 mg in 1 PACKAGE; Type 0: Not a Combination Product08/29/201405/02/2017
2NDC:69161-001-02150 mg in 1 PACKAGE; Type 0: Not a Combination Product05/02/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34808/29/2014
Labeler - Lugus Group LLC (079463507)
Registrant - Lugus Group LLC (079463507)
Establishment
NameAddressID/FEIBusiness Operations
Lugus Group LLC079463507label(69161-001)

Revised: 12/2019
Document Id: 99eb0620-bb08-5fa1-e053-2a95a90a03d9
Set id: 2db0b1a3-31c9-4b94-b905-9ff18d5b25e9
Version: 23
Effective Time: 20191217
 
Lugus Group LLC