ARTHRO PHARMA PAIN RELIEF (camphor- synthetic gel

ARTHRO PHARMA PAIN RELIEF by

Drug Labeling and Warnings

ARTHRO PHARMA PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by Jajy Ventures, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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:

INGREDIENTS AND APPEARANCE

ARTHRO PHARMA PAIN RELIEF 
camphor (synthetic) gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71046-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
CINNAMON BARK OIL (UNII: XE54U569EC)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ALCOHOL (UNII: 3K9958V90M)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71046-001-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/01/2016

Labeler - Jajy Ventures, LLC (080417283)