PHOENIX KINETICREAM ANTI-INFLAMMATORY AND PAIN RELIEF- menthol cream 
Pure Source, LLC

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Phoenix KinetiCream Antiflammatory and Pain Relief Cream

Drug Facts

Active Ingredients

Menthol 2.00%

Purpose

Topical Pain Relief

Uses

temporary relieves of these symptoms:

Warnings

For external use only.

Stop use and ask a doctor if:

  • condition worsen
  • pain persist of more than 7 days
  • irritation develops

Avoid contact with eyes and open wounds.

If swallowed, get medical help or contact your local Poison Control Center or emergency room immediately.

If pregnant or breast feeding

ask a health professional before use.

Keep out of reach of children.

Directions

Adults and children 6 years and over:

Inactive ingredients:

Aloe barbadensis (aloe vera gel) juice, aqua (deionized water), arnica montana (arnica) extract, azadirachta indica (neem) oil, bromelain, butyrospermum parkii (shea) butter, C13-14 isoparaffin, camellia sinensis (green tea) leaf extract, cetearyl alcohol, chondroitin sulfate, citric acid, citrus aurantium bergamia (bergamot) fruit oil, dimethyl sulfone (MSM), emu oil, ethylhexylglycerin, glucosamine sulfate, glycerin, glyceryl stearate SE, laureth-7, mentha piperita (peppermint) oil, papain, phenoxyethanol, polyacrylamide, polysorbate-20, salix alba (willow) bark extract, SD-Alcohol 40B, sesamum indicum (sesame) seed oil, stearic acid, theobroma cacao (cocoa butter), tocopheryl acetate (vitamin E), xanthan gum.

Package Labeling:

Tube

PHOENIX KINETICREAM ANTI-INFLAMMATORY AND PAIN RELIEF 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-032
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
ARNICA MONTANA (UNII: O80TY208ZW)  
BROMELAINS (UNII: U182GP2CF3)  
SHEA BUTTER (UNII: K49155WL9Y)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
BERGAMOT OIL (UNII: 39W1PKE3JI)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
EMU OIL (UNII: 344821WD61)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
LAURETH-7 (UNII: Z95S6G8201)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
PAPAIN (UNII: A236A06Y32)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
WILLOW BARK (UNII: S883J9JDYX)  
SESAME OIL (UNII: QX10HYY4QV)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
COCOA BUTTER (UNII: 512OYT1CRR)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65121-032-04118 mL in 1 TUBE; Type 0: Not a Combination Product02/07/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01705/22/2013
Labeler - Pure Source, LLC (080354456)
Establishment
NameAddressID/FEIBusiness Operations
Pure Source, LLC080354456manufacture(65121-032)

Revised: 11/2023
Document Id: 0973e425-f377-5656-e063-6394a90acb15
Set id: c28cd0d6-8db8-425b-9790-f396f76dc7ac
Version: 9
Effective Time: 20231105
 
Pure Source, LLC