No Pain More Gain

Manufacturer
Lugus Group LLC
Effective date
2019-12-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:02:03

Label at a glance#

ProductNo Pain More Gain
Active ingredientMENTHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Menthol (0.1%)

Purpose

Topical Analgesic

OTC - PURPOSE SECTION

Use

For temporary relief of muscle and joint pain associated with arthritis, backaches, strains, sports injuries and muscle stiffness

WARNINGS SECTION

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.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INACTIVE INGREDIENT SECTION

Inactive Ingredients

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

INDICATIONS & USAGE SECTION

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 SECTION

Directions

Apply a small amount directly onto the affected area up to four times a day. A hot sensation occurs when NPMG Roll On starts working. If no heat sensation occurs within 6 hours, increase the amount for the next application. Do not use in children under 12 years of age.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NPMG Roll OnNPMG Roll On

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69161-006-012021-01-29C16284748780-1ba0f9c33-49b0-a910-e053-dadaa90a0b855c7622b7-0605-2459-e053-2991aa0a3cff

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69161-006-01No Pain More Gain50 mg in 1 BOTTLELIQUID503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69161-006NO PAIN MORE GAIN (MENTHOL) LIQUID [LUGUS GROUP LLC]3Legacy NDC, 1 package rows20191218_5c7622b7-0605-2459-e053-2991aa0a3cff.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69161-00669161-006-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
99eb1326-ab0d-3dd5-e053-2a95a90a2cde5c7622b7-0605-2459-e053-2991aa0a3cff2019-12-17WarningsExact identifier
spl id: 99eb1326-ab0d-3dd5-e053-2a95a90a2cde
spl set id: 5c7622b7-0605-2459-e053-2991aa0a3cff

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.