Label: RE-LIEVED LIDOCAINE PATCH- lidocaine patch 4% patch
- NDC Code(s): 71662-000-01, 71662-000-06
- Packager: Transfer Technology
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 11, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Indications & Usage
- Warnings
- Do not use
- When using this product
- Ask your doctor or pharmacist before use if you are
- Stop use or ask a doctor if
- If pregnant or breast feeding
- Keep out of reach of children
- Directions:
- Other information
- Inactive Ingredients
- Relieved 4% Lidocaine Patches, Six per Box
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INGREDIENTS AND APPEARANCE
RE-LIEVED LIDOCAINE PATCH
lidocaine patch 4% patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71662-000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 18 mg in 116 cm2 Inactive Ingredients Ingredient Name Strength ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71662-000-06 6 in 1 CARTON 07/23/2023 1 NDC:71662-000-01 116 cm2 in 1 POUCH; 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 07/23/2023 Labeler - Transfer Technology (037968132) Registrant - Transfer Technology (037968132) Establishment Name Address ID/FEI Business Operations Transfer Technoloy 037968132 manufacture(71662-000)