Label: MAXIMUM STRENGTH PAIN RELIEF LIDOCAINE PATCH- lidocaine patch
- NDC Code(s): 11822-6541-0, 11822-6541-1
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Warnings
- Do not Use
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When using this product
■ use only as directed
■ read and follow all directions and warnings on this carton
■ do not allow contact with the eyes
■ do not use at the same time as other topical analgesics
■ do not bandage tightly or apply local heat (such as heating pads) to the area of use
■ do not microwave
■ 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.
- Stop use and consult a doctor
- Keep out of reach of children and pets.
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Dosage and Administration
Directions Adults and children 12 years of age and over :
■ Clean and dry affected area
■ Carefully remove backing from patch starting at a corner.
■ Apply sticky side of patch to affected area.
■ use one patch for up to 12 hours.
■ Discard patch after single use.
■Children under 12 years of age: consult a physician.
- PREGNANCY OR BREAST FEEDING
- Other Safety Information
- Inactive Ingredients
- Uses
- Uses
- Maximum Strength Pain Relief Lidocaine Patch
-
INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH PAIN RELIEF LIDOCAINE PATCH
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-6541 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 100 g Inactive Ingredients Ingredient Name Strength POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F) PETROLATUM (UNII: 4T6H12BN9U) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) GLYCERIN (UNII: PDC6A3C0OX) KAOLIN (UNII: 24H4NWX5CO) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) TARTARIC ACID (UNII: W4888I119H) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) Product Characteristics Color Score Shape RECTANGLE Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-6541-0 6 in 1 CARTON 03/01/2021 1 1 g in 1 PATCH; Type 0: Not a Combination Product 2 NDC:11822-6541-1 5 in 1 CARTON 03/01/2021 2 1 g 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 03/01/2021 Labeler - Rite Aid Corporation (014578892) Establishment Name Address ID/FEI Business Operations Foshan Aqua Gel Biotech 529128763 manufacture(11822-6541)