The following Structured Product Label (SPL) was submitted to the FDA by Home Aide Diagnostics, Inc. for the product Veltrix (NDC 69379-004). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding information for patients, indications & usage, warnings, warnings and precautions, other safety information, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
PURPOSE: Topical analgesic
ACTIVE INGREDIENTS
Lidocain 4% --------------------------------------------------------------------------------------------------------- Topical analgesic
Menthol 1% --------------------------------------------------------------------------------------------------------- Topical analgesic
INDICATIONS
For the temporary relief of pain of muscles and joints associated with:
DIRECTIONS
Adults and children over 12 years
Apply generously to affected area
Massage into painful area until thoroughly absorbed into skin, repeat as necessary, not more than 3-4 times daily
Store at 20°-25°C (68°-77 °F). Avoid direct sunlight.
WARNINGS
FOR EXTERNAL USE ONLY.
STOP USE AND ASK A DOCTOR IF
INACTIVE INGREDIENTS
aliphatic alcohol; stearic acid; vaseline; peregal; Carmellose; odium; water
Veltrixrx.jpg (Veltrixrx)
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