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Valtrum TOPICAL ANALGESIC

Dosage form
CREAM
Labeler
Laboratorios Quantium LLC
Label updated
2026-05-13
Retrieved
2026-09-07
Active ingredients
CAMPHOR (SYNTHETIC) · MENTHOL, UNSPECIFIED FORM · METHYL SALICYLATE
View original label and images on DailyMed ↗
Drug Facts

Active Ingredients

Camphor 3%

Menthol 3%

Methyl salicylate 10%

Purpose

Topical analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with • Simple Backache • Arthritis • Strains • Bruises • Sprains

Warnings

For external use only

• Avoid contact with eyes and mucous membranes • Do not use otherwise than as directed.

Caution:  Discontinue use if excessive irritation of the skin develops.

When using this product: • Do not bandage tightly • Do not apply to wounds or damaged skin.

Stop use and ask a doctor if:  • Conditions worsens • Symptoms persist for more than 7 days or clear up and occur again within a few days.

Label information

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 right away.

Directions

Adult and Children 18 years of age and older:  Apply to affected area not more than 3 to 4 times daily. Children under 18 years of age: Consult a doctor.

Other information

• Store in a cool dry place away from direct sunlight • Keep lid tightly closed

Inactive Ingredients:

Arnica Montana Extract, Cat's Claw Extract, Cetyl Stearyl Alcohol, Chuchuhuasi Extract, Devil's Claw Extract, DMDM Hydantoin, Ether, Glucosamine Sulfate, Mineral Oil, PEG-20 Cetyl/Stearyl Ether, Polysorbate 20, Purified Water, Sodium Hydroxide, Stearyl Alcohol, Tocopheryl Acetate.

Label information

POWERFUL ANALGESIC

NEW CREAM

santo remedio IMMEDIATE ACTION 

Creamy Natural Beige

Distributed in the USA by:
LABORATORIOS QUANTIUM MIAMI - FL-USA

Customer Service: +1786-956-0812

[email protected]

Packaging

[Image in the official label — see DailyMed source]

DailyMed Set ID: f3c4cc3a-f3a3-4d02-97e0-9c3fc1a67c3e · Version 1
NDC: 75849-031