PROSTADERM- camphor plaster 
EZP Corporation

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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Prostaderm

Active ingredients                         Purpose

Camphor 3%...........................External analgesic

Uses For the temporary relief of pain

When using this product

Stop use and ask a doctor if

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

Keep this and all drugs out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away
Do not use otherwise than as directed

Directions

AdultsApply to affected area for 24-48 hours
Children under 18 years of ageAsk a doctor

For external use only.

Do not use otherwise than as directed

Uses For the temporary relief of pain.

Cistanche Deserticola stem, Syzygium aromaticum whole, Commiphora myrrha resin, Corydalis bungeana whole, Dictamnus dasycarps root bark, Foeniculum vulgare whole, Synthetic moschus resin, Polyvinyl alcohol, Glycerol, Laurocapram

Prostaderm PDP

Prostaderm PDP

Prostaderm Drug Facts

Prostaderm Drug Facts

PROSTADERM 
camphor plaster
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69446-100
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)3   in 100 
Inactive Ingredients
Ingredient NameStrength
CISTANCHE DESERTICOLA STEM (UNII: 45BEI4ZF64)  
SYZYGIUM AROMATICUM WHOLE (UNII: EY9MMA0P6Y)  
COMMIPHORA MYRRHA WHOLE (UNII: UU81N77RI7)  
CORYDALIS BUNGEANA WHOLE (UNII: 732H9A883V)  
DICTAMNUS DASYCARPUS ROOT BARK (UNII: LA97176ILS)  
FOENICULUM VULGARE WHOLE (UNII: J1UK54JBGH)  
MOSCHUS MOSCHIFERUS MUSK SAC RESIN (UNII: 8KFK4W7KP7)  
POLYVINYL ALCOHOL (UNII: 532B59J990)  
GLYCEROL FORMAL (UNII: 3L7GR2604E)  
LAUROCAPRAM (UNII: 1F3X9DRV9X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69446-100-011 in 1 PACKAGE02/24/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/24/2015
Labeler - EZP Corporation (039212541)
Registrant - Jinzhou Zijing Pharmaceutical Co. (527929247)
Establishment
NameAddressID/FEIBusiness Operations
Jinzhou Zijing Pharmaceutical Co., Ltd.527929247manufacture(69446-100)

Revised: 2/2015
Document Id: a2d1609e-8274-4e19-855f-03a787a3888c
Set id: b6fe33fa-8c06-4280-be21-b5319dab990a
Version: 1
Effective Time: 20150224
 
EZP Corporation