Label: NO PAIN MORE GAIN- menthol cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69161-001-01, 69161-001-02 - Packager: Lugus Group LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated December 17, 2019
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- ACTIVE INGREDIENT
- PURPOSE
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- DOSAGE & ADMINISTRATION
- WARNINGS
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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)
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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.
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INGREDIENTS AND APPEARANCE
NO PAIN MORE GAIN
menthol creamProduct 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)
