DR. SPENSERS NATURAL HERBAL PAIN RELIEF - menthol cream 
LTC Health Corp

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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Active Ingredient

Menthol (Mentha piperita 3.5%, from leaf and aerial parts)

Purpose

Natural Herbal Pain Relief Cream

Keep out of reach of children

Keep out of reach of children.

Indications:

For the temporary relief of aches and pains of muscles and joints associated with arthritis, strains, sprains, bruises and backache.

Warnings:

For external use ONLY. If rash or irritation occurs, discontinue use. The application of eternal heat such as an electric heating pad may result in excessive skin irritation or skin burn. Avoid contact with eyes, mucous membranes, and damaged skin or open wound. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician.

Do not use

if you are pregnant or breast feeding.

Directions:

Adults and children 12 years of age and older: Apply and massage a small amount 3 times over the area of pain. Repeat 3 to 4 times daily.

Non-medicinal Ingredients:

purified water, herbal extracts of : ledebouriella root, sophora root, acanthopanax root, knotweed root, chebula, dandelion, isopropyl alcohol, sunflower oil, emulsifying wax, ethoxydiglycol, isopropyl myristate, carbomer, optiphen plus, phenoxyethanol, BHT, sodium hydroxide

Dr. Spenser's Product Label

Dr. Spenser's™

Natural Herbal Pain Relief Cream

Pain Relief

    Arthritis
    Backache
    Bruise
    Sprains
    Strains

NPN 80013022  75g

Manufactured by:
LTC Health Corp.
Richmond, BC, Canada V6X 1A3

www.DrSpensers.com

LTC drspenser Label

DR. SPENSERS NATURAL HERBAL PAIN RELIEF 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69562-022
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM2.625 g  in 75 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)  
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
ELEUTHERO (UNII: ZQH6VH092Z)  
PERSICARIA TINCTORIA LEAF (UNII: FU6582QMPV)  
TERMINALIA CHEBULA FRUIT (UNII: S8R4V700NK)  
TARAXACUM OFFICINALE (UNII: 39981FM375)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
PEG-150 STEARATE (UNII: 7BSG7DF10Q)  
STEARETH-20 (UNII: L0Q8IK9E08)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69562-022-0175 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35611/01/2009
Labeler - LTC Health Corp (202782066)
Registrant - LTC Health Corp (202782066)
Establishment
NameAddressID/FEIBusiness Operations
LTC Health Corp202782066manufacture(69562-022)

Revised: 1/2015
Document Id: 85d11e40-f0bc-45b9-94dc-e84456191eda
Set id: 0398e9ef-5720-49d6-96c0-56603d330045
Version: 1
Effective Time: 20150116
 
LTC Health Corp