COPPERGEL- camphor, menthol gel 
CopperRelief, LLC

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.

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CopperGel

DRUG FACTS:

ACTIVE INGREDIENTS:

Camphor 3.5%

Menthol 3.5%

Purpose:

Topical Analgesic

USES: for the temporary relief of minor aches and pains in muscles and joints associated with:

WARNINGS:

For external use only.

Do not use

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding, ask a health professional before use.

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

DIRECTIONS:

INACTIVE INGREDIENTS: Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Blue 1, Copper PCA, Ethylhexylglycerin, Eucalyptus Globulus (Eucalyptus) Leaf Oil, Isopropyl Alcohol, Phenoxyethanol, Triethanolamine, Water (Aqua)

Distributed By: Copper Relief, LLC

Wayzata, MN 55391

www.coppergel.com

MADE IN THE USA

CopperGel

KNOCK OUT THE PAIN™
Topical Analgesic Gel

NET WT. 3 OZ (85g)

coppergel label

COPPERGEL 
camphor, menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72081-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL3.5 g  in 100 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)3.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
COPPER PIDOLATE (UNII: 497G7G1SL1)  
WATER (UNII: 059QF0KO0R)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72081-001-031 in 1 CARTON02/05/2018
185 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/05/2018
Labeler - CopperRelief, LLC (080979585)

Revised: 2/2018
Document Id: 6469c4e0-af7c-2ab1-e053-2991aa0a85f3
Set id: 6469c4e0-af7b-2ab1-e053-2991aa0a85f3
Version: 1
Effective Time: 20180204
 
CopperRelief, LLC