Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC
Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC is an FDA drug label for the active ingredient CAMPHOR, MENTHOL, METHYL SALICYLATE manufactured by LABORATORIOS QUANTIUM LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231221.
- Generic name
- CAMPHOR, MENTHOL, METHYL SALICYLATE
- Manufacturer
- LABORATORIOS QUANTIUM LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 75849-897
- Application
- M017
- Label effective
- 20231221
Active ingredients
Indications & Usage
Uses For the temporary relief of minor aches and pains of muscles and joints associated with • Simple Backache • Arthritis • Strains • Bruises • Sprains
Dosage & Administration
Directions Adults 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.
Contraindications
Not available.
Warnings
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. 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.
Adverse Reactions
Not available.