PAIN RELIEVING MUSFLEX  - camphor (natural), menthol lotion 
CHUNG KEE USA INTERNATIONAL INC

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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Pain Relieving Lotion MUSFLEX

Pain Relieving Lotion MUSFLEX


Active Ingredients

Camphor 5.6%

Menthol 5.6%

Purpose

External Analgesic

Uses

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

Warnings

For external use only.

Avoid contact with the eyes.

Do not use

  • on wounds or damaged skin

When using this product

  • do not bandage tightly

Stop use and ask a doctor if

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children to prevent accidental poisoning.

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other Information

Inactive Ingredients

Ethanol, Water, Ramulus Cinnamomi, Radix Notoginseng, Radix Angelicae Pubuscentis, Rhizoma Et Radix Pol Ygoni Cuspidati, Flos Carthami, Rhizoma Zedoariae

Manufactured By:

Nan San (HK) Pharmaceutical Factory Limited

Unit C1, 10/f, Hoi Bun

Industrial Building, 6 Wing Yip Street,

Kwun Tong, Hong Kong, China.

Distributed By:

CHUNG KEE USA
INTERNATIONAL INC
BROOKLYN, NY 11238

Pain Relieving Lotion MUSFLEX


MusflexOuterPackage

InnerPackage

DrugFacts

PAIN RELIEVING MUSFLEX  
camphor (natural), menthol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55424-1398
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)56 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL56 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
OCIMUM GRATISSIMUM LEAF OIL (UNII: AVG2506KDV)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
WATER (UNII: 059QF0KO0R)  
CHINESE CINNAMON (UNII: WS4CQ062KM)  
PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)  
ANGELICA BISERRATA ROOT (UNII: OJ90180B22)  
SAFFLOWER (UNII: 4VBL71TY4Y)  
ZEDOARY (UNII: 123C43G128)  
POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55424-1398-880 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34801/09/2013
Labeler - CHUNG KEE USA INTERNATIONAL INC (016224514)
Establishment
NameAddressID/FEIBusiness Operations
Nan San (HK) Pharmaceutical Factory Limited666458539manufacture(55424-1398)

Revised: 1/2013
Document Id: 191734b3-f360-4e02-9211-52c127c94788
Set id: bc27a8df-49be-4d73-ba2c-2b10c1f7ad91
Version: 2
Effective Time: 20130111
 
CHUNG KEE USA INTERNATIONAL INC