Label: LIDOPATCH- lidocaine hcl, menthol patch
- NDC Code(s): 10882-528-01, 10882-528-03, 10882-528-30
- Packager: JAR Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 25, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
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INDICATIONS & USAGE
Temporarily relieves minor pain associated with: arthritis, simple backache, bursitis, tendonitis, muscle strains, sprains & bruises.
LidoPatch
contains lidocaine
PAIN RELIEF PATCHFor minor pain associated with
arthritis
back pain
muscle sprains & strains
The only over the counter patch with lidocaine
ultra thin, flexible, trim to fit -
Warnings
For external use only. Do not use if you are allergic or sensitive to lidocaine or menthol. Do not use if pouch is damaged or opened.
Handling and Disposal
- hands should be washed after the handling and eye contact should be avoided
- do not store patch outside the sealed envelope
- apply immediately after removal from protected envelope
- fold used patches so that the adhesive side sticks to itself and safely discard used patches or pieces of cut patches where children and pets cannot get them
- kept out of the reach of children both before and after use
Stop use and ask a doctor if
- excessive redness or irritation is present
- condition worsens
- pain persists for more than 7 days
- symptoms clear up and occur again within a few days
If pregnant or br east-feeding, ask a health professional before use.
- Directions
- KEEP OUT OF REACH OF CHILDREN
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LIDOPATCH
lidocaine hcl, menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10882-528 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 505 mg MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 175 mg Inactive Ingredients Ingredient Name Strength PROPYLPARABEN (UNII: Z8IX2SC1OH) CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) WATER (UNII: 059QF0KO0R) METHYLPARABEN (UNII: A2I8C7HI9T) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) TARTARIC ACID (UNII: W4888I119H) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10882-528-01 1 in 1 BOX; Type 0: Not a Combination Product 10/29/2015 10/31/2023 2 NDC:10882-528-03 3 in 1 BOX; Type 0: Not a Combination Product 10/29/2015 10/31/2023 3 NDC:10882-528-30 30 in 1 BOX; Type 0: Not a Combination Product 10/29/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 10/29/2015 Labeler - JAR Laboratories (968952239)