PAIN RELIEVING ARTHRITIS- histamine dihydrochloride cream 
Velocity Pharma 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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Pain Relieving Arthritis Cream- RA

Drug Facts

Active Ingredient

Histamine dihydrochloride ...... 0.025%

Purpose

External Analgesic

Uses

Warnings

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

Directions

Other information

Inactive ingredients

arylamide, butylated hydroxyl toluene, cetostearyl alcohol , cetomacrogol 1000, disodium EDTA, glucosamine sulfate, glycerin, isohexadecane, polysorbate 80,  propylene glycol, sodium acrylodimethyl taurate copolymer, titanium dioxide, transquitol P, vitamin E acetate,  white petroleum jelly, water

Questions or Comments? Call 1855-314-1850

Distributed by: Velocity Pharma LLC 
Farmingdale, NY, 11735

Pain Relieving Arthritis Cream

Net Wt. 4 oz (119g)

ra Arthritis

PAIN RELIEVING ARTHRITIS 
histamine dihydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76168-300
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE0.025 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ACRYLAMIDE (UNII: 20R035KLCI)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DISODIUM HYDROGEN CITRATE (UNII: 6FO62KCQ7A)  
EDETATE SODIUM (UNII: MP1J8420LU)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
PETROLATUM (UNII: 4T6H12BN9U)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76168-300-38119 g in 1 JAR; Type 0: Not a Combination Product05/26/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/26/2017
Labeler - Velocity Pharma LLC (962198409)
Registrant - Velocity Pharma LLC (962198409)
Establishment
NameAddressID/FEIBusiness Operations
Yash Pharmceuticals871409551manufacture(76168-300)
Establishment
NameAddressID/FEIBusiness Operations
Velocity Pharma LLC962198409label(76168-300)

Revised: 5/2017
Document Id: 506e9e32-22d7-0c25-e054-00144ff88e88
Set id: 20137af7-3494-45c6-97e1-f6ecef6354af
Version: 2
Effective Time: 20170526
 
Velocity Pharma LLC