FDA.reportPublic FDA data

ARTHRO PHARMA PAIN RELIEF GEL

Manufacturer
Jajy Ventures, LLC
Effective date
2019-03-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:28:39

Label at a glance#

ProductARTHRO PHARMA PAIN RELIEF
Active ingredientCAMPHOR (SYNTHETIC)
Label structure7 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.00%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS:

INDICATIONS & USAGE SECTION

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

WARNINGS:

WARNINGS SECTION

  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, consult physician.
  • Do not apply to wounds or damaged skin.
  • Do not bandage tightly.

If pregnant or breast feeding, 

OTC - PREGNANCY OR BREAST FEEDING SECTION

contact physician prior to use.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

SPL UNCLASSIFIED SECTION

Store at room temperature.

OTHER INGREDIENTS:

INACTIVE INGREDIENT SECTION

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:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71046-00171046-001-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
CENTELLA ASIATICA7M867G6T1UIACT
CINNAMON BARK OILXE54U569ECIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HELICHRYSUM ITALICUM FLOWERP62Y550X24IACT
HYPERICUM PERFORATUMXK4IUX8MNBIACT
MALTODEXTRIN7CVR7L4A2DIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
ALCOHOL3K9958V90MIACT
SODIUM HYDROXIDE55X04QC32IIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
071dcae0-303e-2684-e063-6394a90a33b2403f5614-eccd-1189-e054-00144ff8d46c2023-10-07WarningsExact identifier
spl set id: 403f5614-eccd-1189-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.