LIBERDOL TOPICAL ANALGESIC (methyl salicylate, menthol, camphor- synthetic spray

Liberdol Topical Analgesic by

Drug Labeling and Warnings

Liberdol Topical Analgesic by is a Otc medication manufactured, distributed, or labeled by ViaDerma Distribution, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Methyl Salicylate 300mg

Menthol 100mg

Camphor 40mg

Purpose

Analgesic

Uses

Soothing on-the-go tempoary relief from minor aches and pains of sore muscles and joint associated with:

• arthritis
• backache
• strains
• sprains

Warnings

For external use only. : Keep away form excessive heat or open flame Flammable

Ask a doctor before use if you have:

Sensitive skin, are pregnant or are bleeding

When using this product:

• Avoid contact with eyes or mucus membranes
• Do not apply to open wounds or damaged skin
• Do not use with other ointments, creams, sprays or liniments
• Do not apply to irritated skin, or if excessive irritation develops
• Do not bandage
• Do not use with heating pad or device

Stop use and ask a doctor if:

Condition worsens or if symptoms persist more than 7 days, or clear up or reoccur

Keep out of reach of children.

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

Directions

• Apply to affected areas not more than 4 times daily Adults and children 2 years of age an older: 
• Consult a physician Children under 2 years of age:

Other Information

• Store in a cool dry place out of direct sunlight

Inactive Ingredients

acetic acid, arnica montana flower extract, ascorbic acid, chlorhexidine gluconate, cholecalciferol, dimethyl sulfoxide, dipropylene glycol, glucono delta lactone, glycerin, histidine, hydroxethyl cellulose, magnesium stearate, sodium hydroxide, sorbic acid, stearic acid, water

Package Labeling:

INGREDIENTS AND APPEARANCE

LIBERDOL TOPICAL ANALGESIC 
methyl salicylate, menthol, camphor (synthetic) spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71262-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	300 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	100 mg  in 1 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACETIC ACID (UNII: Q40Q9N063P)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
GLYCERIN (UNII: PDC6A3C0OX)
HISTIDINE (UNII: 4QD397987E)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SORBIC ACID (UNII: X045WJ989B)
STEARIC ACID (UNII: 4ELV7Z65AP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71262-008-55	1 in 1 CARTON	06/01/2021
1		55 mL in 1 BOTTLE; 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	06/01/2021

Labeler - ViaDerma Distribution, Inc (081113521)