DeeDol Topical Analgesic Spray

DeeDol Topical Analgesic by

Drug Labeling and Warnings

DeeDol Topical Analgesic by is a Otc medication manufactured, distributed, or labeled by MATRIX MIXOLOGY, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DEEDOL TOPICAL ANALGESIC- methyl salicylate, menthol, camphor (synthetic) spray 
MATRIX MIXOLOGY, INC

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DeeDol Topical Analgesic Spray

Drug Facts

Active Ingredient (in each gram)

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, vreams, sprays or liniments ■ Do not apply to irritaed 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 ■ Consult a physician Adults and children 2 years of age an older: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:118ml

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79218-003
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: 79218-003-01	1 in 1 BOX	12/31/2020	12/09/2024
1		118 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	12/31/2020	12/09/2024

Labeler - MATRIX MIXOLOGY, INC (128885636)

Revised: 12/2024

Document Id: 29280d1c-2349-2ec2-e063-6394a90af456

34390-5

Set id: c67f5610-9ca3-427e-8ad4-6e04917d67fb

Version: 3

Effective Time: 20241213