Label: LIDOPRO PATCH- lidocaine, menthol, and methyl salicylate patch
- NDC Code(s): 83881-401-02, 83881-401-30
- Packager: Clinic Pharma
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 11, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Uses
-
Warnings
For external use only
Do not use
• more than one patch on your bidy at a time or on cuts, irritated, or swollen skin
• on puncture wounds
• for more than one week without consulting a doctor.
When using this product
- Use only as directed. Read and follow directions and warning on this packaging.
- Do not apply to wounds or damaged, broken, or irritated skin
- Avoid contact with the eyes or mucous membranes
- Do not bandage tightly or apply local heat (such as heating pads) to area of use
- Do not use at the same time as other topical analgesics
- Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.
- DIRECTIONS
- OTHER INGREDIENTS:
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
LIDOPRO PATCH
lidocaine, menthol, and methyl salicylate patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83881-401 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 mg in 100 mg MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.5 mg in 100 mg METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 0.1 mg in 100 mg Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W) POLYSORBATE 80 (UNII: 6OZP39ZG8H) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83881-401-30 15 in 1 BOX 02/09/2024 1 2 in 1 POUCH 1 8500 mg in 1 PATCH; Type 0: Not a Combination Product 2 NDC:83881-401-02 2 in 1 POUCH 02/09/2024 2 8500 mg in 1 PATCH; 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 02/09/2024 Labeler - Clinic Pharma (119158469)