Label: ARTHCAL 4% LIDOCAINE PATCHES- lidocaine patch
- NDC Code(s): 85212-0004-1
- Packager: Beijing JUNGE Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 22, 2025
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- Official Label (Printer Friendly)
- DRUG FACTS
- ACTIVE INGREDIENT
- USE
-
WARNINGS
For external use only
Do not use
more than 1 patch at a time
with a heating pad
on wounds or damaged skin
ir you are allergic to any ingredients of this product
When using this product
use only as directed
do not bandage tightly
avoid contact with the eyes, mucous membranes or rashes
Stop use and ask a doctor if
symptoms persist for more than 7 days
conditions worsen
symptoms clear up and occur again within a few days
localized skin reactions, such as rash, itching, redness, pain, swelling and blistering develop
If pregnant or breast feeding,
ask a health professional before use
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away. - DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ARTHCAL 4% LIDOCAINE PATCHES
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85212-0004 Route of Administration EXTRACORPOREAL 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 WATER (UNII: 059QF0KO0R) 37 g in 100 g GLYCERIN (UNII: PDC6A3C0OX) 11 g in 100 g PROPYLPARABEN (UNII: Z8IX2SC1OH) 6 g in 100 g METHYLPARABEN (UNII: A2I8C7HI9T) 0.5 g in 100 g POLYSORBATE 80 (UNII: 6OZP39ZG8H) 9 g in 100 g DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K) 6 g in 100 g TARTARIC ACID (UNII: W4888I119H) 0.5 g in 100 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 2 g in 100 g POVIDONE K90 (UNII: RDH86HJV5Z) 8 g in 100 g KAOLIN (UNII: 24H4NWX5CO) 10 g in 100 g PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 6 g in 100 g Product Characteristics Color Score Shape Size 140mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85212-0004-1 7 g in 1 BOX; Type 0: Not a Combination Product 10/01/2024 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 10/01/2024 Labeler - Beijing JUNGE Technology Co., Ltd. (848718652) Registrant - Beijing JUNGE Technology Co., Ltd. (848718652) Establishment Name Address ID/FEI Business Operations Zhejiang Ayan Biotech Co., Ltd. 544377996 manufacture(85212-0004)
