FORMULA45 ARTHRITIS BLEND- methyl salicylate, menthol, unspecified form cream 
Shift Consulting Group, Inc.

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Formula45 Arthritis Blend

Drug Facts:

Active Ingredient:

Methyl Salicylate 20.00%

Menthol 10.00%

Purpose:

Topical Analgesic

Indications:

For the temporarily relief of minor aches and pains of the muscles and joints associated with

  • simple backache
  • arthritis
  • strains
  • bruises
  • and sprains

Warnings:

For external use only

Allergy Alert: If you had prior allergic reaction to aspirin or salicylate, please consult a physician before use.

Do not use

  • on wounds or damaged skin
  • with a heating pad
  • children 12 years of age with arthritic conditions

Ask a physician before use if

you have redness over the affected area.

When using this product

  • avoid contact with eyes and mucus membranes
  • do not bandage highly

Stop use and ask a physician if

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clearup and occur again within a few days
  • excessive skin irritation occurs.

If pregnant or breastfeeding,

ask a health professional before use.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions:

Use only as directed

  • Adults and children over 12 years of age apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age consult a physician.

Other Ingredients:

Aqua (deionized water), arnica montana (arnica) extract, blue 1, boswellia serrata extract, C13-14 isoparaffin, cetyl alcohol, chondroitin sulfate, dimethyl sulfone (MSM), ethylhexylglycerin, glucosamine sulfate, glycerin, glyceryl stearate, laureth-7, PEG-100 stearate, phenoxyethanol, polyacrylamide, polysorbate-20, stearic acid, yellow 5.

Package Labeling:

Label

FORMULA45 ARTHRITIS BLEND 
methyl salicylate, menthol, unspecified form cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70169-701
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE200 mg  in 1 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM100 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ARNICA MONTANA (UNII: O80TY208ZW)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
LAURETH-7 (UNII: Z95S6G8201)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70169-701-011 in 1 CARTON02/07/201702/07/2017
1113 g in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01710/16/201502/07/2017
Labeler - Shift Consulting Group, Inc. (079991681)

Revised: 10/2023
 
Shift Consulting Group, Inc.