Label: WALGREENS LIDOCAINE BACK- lidocaine patch
- NDC Code(s): 0363-2178-01
- Packager: Walgreen Co.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 14, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Use
-
Warnings
For external use only
Do not use
- More than one patch on your body at a time
- On cut, irritated or swollen skin
- On puncture wounds
- For more than one week without consulting a doctor
- If you are allergic to any active or inactive ingredients
- If pouch is damaged or opened
When using this product
- Use only as directed
- Read and follow all directions and warnings
- Do not allow contact with the eyes
- Do not use at the same time as other topical anesthetics
- 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.
-
Directions
Adults and children 12 years if age and over:
- Clean and dry affected area
- Carefully remove backing from patch
- Apply sticky side of patch to affected area
- Use one patch for up to 8 hours
- Discard patch after single use
- Apply 1 patch at a time to affected area, not more than 3 to 4 times daily
Children under 12 years of age:consult a physician.
- Other information
-
Inactive ingredients
A-tocopherol Acetate, CMC-2Na, Dihydroxyaluminum Aminoacetate, Fumed Silica, Glycerol, Laurocapram, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Polyacrylic Acid, Propylene Glycol, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Urea, Vanillyl Butyl Ether, Water, 3-2-(Ethylhexyl)oxyl-1, 2-Propanediol.
- Package Labelling:
-
INGREDIENTS AND APPEARANCE
WALGREENS LIDOCAINE BACK
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-2178 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg in 1 g Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) GLYCERIN (UNII: PDC6A3C0OX) LAUROCAPRAM (UNII: 1F3X9DRV9X) PEG-40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TARTARIC ACID (UNII: W4888I119H) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) UREA (UNII: 8W8T17847W) VANILLYL BUTYL ETHER (UNII: S2ULN37C9R) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-2178-01 6 in 1 BOX 10/20/2024 1 1 in 1 BAG 1 7 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 10/20/2024 Labeler - Walgreen Co. (008965063)