Label: NO PAIN MORE GAIN- menthol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69161-006-01 - Packager: Lugus Group LLC
- Category: HUMAN OTC DRUG LABEL
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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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
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INDICATIONS & USAGE
100% Vegan
No Pain More Gain
Roll On
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) Roll On 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 Roll On is a product of
Lugus Group LLC Buffalo, WY 82834, USA
NET WT. 1.6 fl oz (50 ml)
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NO PAIN MORE GAIN
menthol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69161-006 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 SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) BAMBUSA VULGARIS STEM (UNII: SMR633LHTC) HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR) GERANIOL (UNII: L837108USY) BENZYL BENZOATE (UNII: N863NB338G) LINALOOL, (-)- (UNII: 3U21E3V8I2) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) HORDEUM VULGARE TOP (UNII: 86507VZR9K) SORBITOL (UNII: 506T60A25R) LIMONENE, (+)- (UNII: GFD7C86Q1W) WATER (UNII: 059QF0KO0R) CITRAL (UNII: T7EU0O9VPP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) VANILLYL BUTYL ETHER (UNII: S2ULN37C9R) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69161-006-01 50 mg in 1 BOTTLE; Type 0: Not a Combination Product 10/23/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 10/23/2017 Labeler - Lugus Group LLC (079463507) Registrant - Lugus Group LLC (079463507) Establishment Name Address ID/FEI Business Operations Lugus Group LLC 079463507 label(69161-006)