BIO-RELIEF- menthol gel 
Scientific Solutions Global LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Label

Menthol 10%

Topical Analgesic

For temporary relief of minor aches and pains of muscles and joints associated with • simple backache • arthritis • strains• bruises • sprains

For external use only. Flammable, keep away from fire/flame.

Keep out of reach of children, if swallowed, get medical help or contact a Poison Control Center right away.

Adults & children 2 yrs of age and older: Apply to affected area not more than 4 times daily in one direction, not circular. Children under 2 years of age, consult a physician. Massage not necessary. Shake well before use.

Aloe Vera Oil, Arnica Flower Tincture, Boswellia Powder, Camphor, Frankincense Oil, Green Tea, Hydroxypropyl Cellulose NF, Isopropyl Alcohol, Lavender Oil, Propylene Glycol, Tea Tree Oil, Thymol, Vitamin E.

Store in a cool and dry place with lid closed tightly.

Questions or Comments? E-mail: info@scisolglobal.com Manufactured and Distributed by: Scientific Solutions Global LLC, Carle Place, NY, USA

BIO-RELIEF 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71718-200
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM8.9 g  in 89 mL
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
ARNICA MONTANA (UNII: O80TY208ZW)  
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
TEA TREE OIL (UNII: VIF565UC2G)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
THYMOL (UNII: 3J50XA376E)  
Product Characteristics
Colorwhite (Opaque gel) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71718-200-0189 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/01/2020
Labeler - Scientific Solutions Global LLC (097291290)
Registrant - Scientific Solutions Global LLC (097291290)
Establishment
NameAddressID/FEIBusiness Operations
Scientific Solutions Global LLC097291290manufacture(71718-200)

Revised: 2/2020
Document Id: 9e541811-0a2e-310f-e053-2a95a90ad5b0
Set id: 9e541811-0a2d-310f-e053-2a95a90ad5b0
Version: 1
Effective Time: 20200211
 
Scientific Solutions Global LLC