BALSANG PAIN RELIEF- camphor,menthol, methyl salicylate solution 
Genuine Drugs

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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Balsang Pain Relief

Active Ingredients

Camphor 1.5%

Menthol 1.5%

Methyl salicylate 5%

Uses

For the temporarily relieves minor aches and pains of muscle and joints associated with

For external use only.

When using this product

  • use only as directed
  • avoid contact with eyes and mucous membranes
  • do not apply to wounds, damaged or irritated skin
  • do not bandage or cover with wrap or use heating pad
  • do not use 1 hour prior to bathing or 30 minutes after bathing

Stop use and ask a doctor if

  • condition worsens
  • severe skin irritation occurs
  • pain persists for more than 7 days
  • pain clears up and then reocurs a few days later.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately

If pregnant or breast-feeding

ask a health professional before use

Directions

Other information

Inactive Ingredients

Cajuput Oil, Chondroitin Sulfate, Cinnamon Oil, Clove Oil, Deionized Water, Dementholised Mint Oil, Deazolidinyl Urea, Glucosamine Sulfate, Methyl Paraben, Methylsulfonylmethane (MSM), PEG-12 Methyl Glucose Dioleate, Propyl Paraben, Propylene Glycol

Pain Reliever

Pain Reliever

Pain Reliever

Balsang Pain Relief

carton

BALSANG PAIN RELIEF 
camphor,menthol, methyl salicylate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69666-962
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, (+)- (UNII: C6B1OE8P3W) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, (+)-1.5 mg  in 100 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE5 mg  in 100 mL
CAMPHOR, (-)- (UNII: 213N3S8275) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR, (-)-1.5 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CAJUPUT OIL (UNII: J3TO6BUQ37)  
CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)  
CINNAMON OIL (UNII: E5GY4I6YCZ)  
CLOVE OIL (UNII: 578389D6D0)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69666-962-041 in 1 BOX04/20/2015
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/20/2015
Labeler - Genuine Drugs (079610378)

Revised: 2/2023
Document Id: f4ee870c-a1de-1d42-e053-2a95a90ada2d
Set id: 142c6ff2-71cd-0f4e-e054-00144ff88e88
Version: 4
Effective Time: 20230217
 
Genuine Drugs