ARTRIDON GLUCOSAMINE- menthol, methyl salicylate ointment

Artridon by

Drug Labeling and Warnings

Artridon by is a Otc medication manufactured, distributed, or labeled by Pharmadel LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients and Purpose

• Active ingredients: Purpose
• Menthol 2%...............................:

  Topical analgesic

• Methyl Salicylate 15% ...............:

  Topical analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with

• simple backaches
• arthritis
• strains
• bruises
• sprains

Warnings

For external use only. Avoid contact with the eyes.

When using this product

• do not apply on wounds or damaged skin
• do not bandage tightly

Stop use and ask a doctor if

• condition worsens
• symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

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: do not use, consult a doctor

Other information

• store between 68-77°F (20-25°C)
• don’t use if foil seal under cap is broken, torn, or missing

Inactive ingredients

bromelains, cetyl alcohol, diazolidinyl urea, dimethicone, dimethyl sulfone, glucosamine, glycerin, isopropyl myristate, medium-chain triglycerides, mineral oil, potassium sorbate, propylene glycol, sorbic acid, xanthan gum, water

Dist by:

PHARMADEL LLC

New Castle, DE, 19720

Questions? +1-866-359-3478

Principal Display Panel

INGREDIENTS AND APPEARANCE

ARTRIDON  GLUCOSAMINE
menthol, methyl salicylate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55758-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	2 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
GLUCOSAMINE (UNII: N08U5BOQ1K)
XANTHAN GUM (UNII: TTV12P4NEE)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CETYL ALCOHOL (UNII: 936JST6JCN)
MINERAL OIL (UNII: T5L8T28FGP)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
BROMELAINS (UNII: U182GP2CF3)
SORBIC ACID (UNII: X045WJ989B)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55758-030-05	1 in 1 CARTON	11/04/2024
1		142 g in 1 TUBE; 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	11/04/2024

Labeler - Pharmadel LLC (030129680)