Label: 4% LIDOCAINE PATCHES patch
- NDC Code(s): 87794-008-01
- Packager: Shenzhen Chaoxiji Technology Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 28, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Use
- Warnings
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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
▪ Dispose of used patch in a 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.
- Do not use
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Stop use and consult a doctor if
▪Condition worsens
▪Redness is present
▪Irritation develops
▪Symptoms persist for more than 7 days or clear up and occur again within a few days
▪You experience signs of skin injury, such as pain, swelling or blistering where the product was applied.
If pregnant or breastfeeding, ask a health professional before use.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
4% LIDOCAINE PATCHES
4% lidocaine patches patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:87794-008 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 Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALUMINUM GLYCINATE (UNII: 1K713C615K) GLYCERIN (UNII: PDC6A3C0OX) RICINUS COMMUNIS (CASTOR) SEED OIL (UNII: D5340Y2I9G) CELLULOSE GUM (UNII: K679OBS311) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) TARTARIC ACID (UNII: W4888I119H) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SILICA (UNII: ETJ7Z6XBU4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) UREA (UNII: 8W8T17847W) POLYACRYLIC ACID (800000 MW) (UNII: D0I6NSZ87U) DMDM HYDANTOIN (UNII: BYR0546TOW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:87794-008-01 40 in 1 BOX; Type 0: Not a Combination Product 08/27/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/27/2026 Labeler - Shenzhen Chaoxiji Technology Co.,Ltd. (511200541) Establishment Name Address ID/FEI Business Operations Shenzhen Chaoxiji Technology Co.,Ltd. 511200541 manufacture(87794-008)

