NO PAIN MORE GAIN- menthol spray 
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, strains, sports injuries and muscle stiffness

Keep out of reach of children

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

Inactive Ingredients

Alcohol, Bambusa Vulgaris Shoot Extract, Benzyl Benzoate, Citral, Citronellol, Geraniol, Glycerin, Hordeum Vulgare Leaf Extract, Hydroxycitronellal, Limonene, Linalool, Parfum, Propylene Glycol, Sodium Polyacrylate,Sorbitol, Vanillyl Butyl Ether, Water, Xanthan Gum

Warnings

• For external use only • Avoid contact with the eyes and mucous membranes • Do not use on irritated skin • Do not wrap, bandage, or use a heating pad on the treated area • Do not use on open wounds or broken skin.

100% Vegan

No Pain More Gain

Hot Spray

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 local noninflammatory pain. No Pain More Gain (NPMG) Hot Spray provides instant pain relief and moisturizes the skin. The natural alternative with the advanced German formula starts to work on contact and relieves pain for hours. NPMG penetrates deeply, absorbs quickly and has a fresh and pleasant scent.

NPMG Hot Spray is a product of

Lugus Group LLC, Buffalo, WY 82834, USA

NET WT 3.4 fl oz (100 ml)

Directions

Spray a small amount directly onto the affected area up to four times a day. Do not use in children under 12 years of age. Wash your hands well after using.

NPMG Hot Spray

NO PAIN MORE GAIN 
menthol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69161-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.1 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
BENZYL BENZOATE (UNII: N863NB338G)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)  
LINALOOL, (-)- (UNII: 3U21E3V8I2)  
ALCOHOL (UNII: 3K9958V90M)  
GERANIOL (UNII: L837108USY)  
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
HORDEUM VULGARE TOP (UNII: 86507VZR9K)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
BAMBUSA VULGARIS STEM (UNII: SMR633LHTC)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SORBITOL (UNII: 506T60A25R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
WATER (UNII: 059QF0KO0R)  
CITRAL (UNII: T7EU0O9VPP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69161-003-01100 mg in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/01/2016
Labeler - LUGUS GROUP LLC (079463507)
Registrant - LUGUS GROUP LLC (079463507)
Establishment
NameAddressID/FEIBusiness Operations
LUGUS GROUP LLC079463507label(69161-003)

Revised: 12/2019
Document Id: 99eafd4a-bf29-f1a1-e053-2a95a90adfae
Set id: 3764bccc-59a1-235c-e054-00144ff8d46c
Version: 12
Effective Time: 20191217
 
LUGUS GROUP LLC