Label: NO PAIN MORE GAIN- menthol aerosol, spray
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Contains inactivated NDC Code(s)
NDC Code(s): 71637-003-01 - Packager: Vema Industrie-verpackung Gmbh & Co. Kg. Kontrakt - Abfullung Und -verpackung
- 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 14, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- ASK DOCTOR
- DOSAGE & ADMINISTRATION
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OTHER SAFETY INFORMATION
Other information
Contents under pressure. Do not expose to sunlight or keep where temperatures exceed 120°F. Do not spray into flames or hot surfaces. Keep away from sources of ignition. Do not puncture or incinerate container. When using this product, keep away from face and mouth to avoid breathing in.
- INACTIVE INGREDIENT
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INDICATIONS & USAGE
100% Vegan
No Pain More Gain
Ice 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 inflammatory and noninflammatory pain. No Pain More Gain (NPMG) provides temporary but long lasting pain relief and moisturizes the skin. The innovative crackling spray contains tiny bubbles. On contact with the skin they burst and release their unique pain relieving properties. NPMG Ice Spray is cold at first, then warm. It can be used selectively, but also on large areas. 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.
Lugus Group LLC, Buffalo, WY 82834, USA
NET WT 5.07 fl oz (150 ml)
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NO PAIN MORE GAIN
menthol aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71637-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5 mg in 100 mg Inactive Ingredients Ingredient Name Strength LINALOOL, (+)- (UNII: F4VNO44C09) HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR) LIMONENE, (+)- (UNII: GFD7C86Q1W) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) BENZYL BENZOATE (UNII: N863NB338G) GERANIOL (UNII: L837108USY) WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) PROPANE (UNII: T75W9911L6) GLYCERIN (UNII: PDC6A3C0OX) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) CITRAL (UNII: T7EU0O9VPP) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) 2-BROMOBUTANE, (S)- (UNII: 2AL1MZU0XA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71637-003-01 150 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/16/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 03/01/2017 Labeler - Vema Industrie-verpackung Gmbh & Co. Kg. Kontrakt - Abfullung Und -verpackung (316193515) Establishment Name Address ID/FEI Business Operations Vema Industrie-verpackung Gmbh & Co. Kg. Kontrakt - Abfullung Und -verpackung 316193515 manufacture(71637-003)
