Zynalox Pain Relief Tape
FDA Label NDC 72835-999
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by V2 Pharma Llc for the product Zynalox Pain Relief Tape (NDC 72835-999). 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 drug facts, active ingredients, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Lidocaine 4%
Purpose
Topical analgesic
Use
for the temporary relief of pain
Warnings
for external use only
When using this product
• use only as directed. Read and follow all directions and warnings on this package
• do not bandage tightly
• avoid contact with eyes and mucous membranes
• do not use at the same time as other topical analgesics
• do not remove when wet or directly after shower, allow to dry and then slowly remove
Stop use and ask a doctor if
• condition worsens
• symptoms persist for more than 7 days or clear up and occur again within a few days
• you experience signs of skin injury, such as pain, swelling or blistering where the tape was applied
• If pregnant or breast-feeding, ask a health professional before use
Otc - Keep Out Of Reach Of Children
• If swallowed, get medical help or contact a Poison Control Center right away
Directions
adults and children over 12 years:
• apply strip for up to 12 hours of wear time
• apply 1 strip at a time to the affected area, not more than 2 to 3 times daily
• store in a cool dry place
children 12 years or younger: ask a doctor
Inactive Ingredients
Acrylic adhesive, Linseed oil, and Polysorbate 80
* Please review the disclaimer below.
