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ARTHRO PHARMA PAIN RELIEF

Dosage form: gel
Ingredients: CAMPHOR (SYNTHETIC) 30mg in 1mL
Labeler: Jajy Ventures, LLC
NDC code: 71046-001

Medically reviewed by Drugs.com. Last updated on Mar 18, 2024.

ARTHRO PHARMA PAIN RELIEF GEL

Drug Facts

ACTIVE INGREDIENT:

Camphor 3.00%

Topical Analgesic

INDICATIONS:

For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and strains.  

WARNINGS:
  • For external use only.
  • Avoid contact with eyes.
  • If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.
  • If swallowed, consult physician.
  • Do not apply to wounds or damaged skin.
  • Do not bandage tightly.

If pregnant or breast feeding, 

contact physician prior to use.

DIRECTIONS:

Adults and children two-years of age or older: Apply to affected area not more than three to four times daily. Children under two-years of age: consult a physician.

ADDITIONAL INFORMATION:

Store at room temperature.

OTHER INGREDIENTS:

Aqua (Deionized Water), Carbomer, Centerlla Asiatica (Gotu Kola) Extract, Cinnamomum Zeylanicum (Cinnamon) Bark Extract, Ethylhexylglycerin, Gaultheria Procumbens (Teaberry) Extract, Harpagophytum Procumbens (Devil's Claw) Extract, Helichrysum Italicum Extract, Hypericum Perfortum (St. John's Wort) Extract, Maltodextrin, Phenoxyethanol, Polysorbate-20, SD-Alcohol, Sodium Hydroxide.

Package Labeling:

ARTHRO PHARMA PAIN RELIEF 
camphor (synthetic) gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71046-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (CAMPHOR (SYNTHETIC)) CAMPHOR (SYNTHETIC)30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CARBOXYPOLYMETHYLENE 
CENTELLA ASIATICA 
CINNAMON BARK OIL 
ETHYLHEXYLGLYCERIN 
HELICHRYSUM ITALICUM FLOWER 
HYPERICUM PERFORATUM 
MALTODEXTRIN 
PHENOXYETHANOL 
POLYSORBATE 20 
ALCOHOL 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:71046-001-04118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/01/2016
Labeler - Jajy Ventures, LLC (080417283)

Document Id: 852b4069-e6f9-3eaa-e053-2a91aa0a69d6
Set id: 403f5614-eccd-1189-e054-00144ff8d46c
Version: 2
Effective Time: 20190328
 
Jajy Ventures, LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer