ARTHRONEO- camphor spray

ArthroNEO by

Drug Labeling and Warnings

ArthroNEO by is a Otc medication manufactured, distributed, or labeled by Likasso LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Camphor 0.50%

Purpose

External Analgesic

Uses

For temporary relief of pain

Warnings

For external use only.

Do Not use

In large quantities, particularly over raw surfaces or blistered areas. If condition worsens or if symptoms persist for more than 7 days or clear up and ocur again within a few days, discontinue use of this product and consult a doctor.

When Using This Product

Avoid contact with the eyes

Stop using and Ask a Doctor

if irritation or rash occurs.

Keep Out Of Reach of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age:
consult a doctor.

Other Information

Keep dry. Store at 5'C and 20'C.

Inactive Ingredients

Sensil CH SP, Amica montana flower extract, Benzyl alcohol, Citric acid, Disodium EDTA, Limonene, Lavandula angustifolia herb oil,
Linalool, Peg-40 hydrogenated castor oil, Potassium sorbate, Propylene glycol, Sodium benzoate, Water

Principal Display

Made in the EU

Manufacturered for Likasso, LTD

Grafenberger Alle 115

4023 Dusseldorf, Germany

NDC: 82312-001-50

INGREDIENTS AND APPEARANCE

ARTHRONEO 
camphor spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82312-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
BENZYL ALCOHOL (UNII: LKG8494WBH)
LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
LINALOOL, (+)- (UNII: F4VNO44C09)
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82312-001-50	1 in 1 BOX	10/27/2021
1		50 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/27/2021

Labeler - Likasso LTD (315086971)