Label: LIDO KING LIDOCAINE 4% PAIN RELIEVING GEL-PATCH- lidocaine patch
- NDC Code(s): 73354-1280-2
- Packager: Galaxy Bio, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 15, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only
Do not use
- if you are allergic to any ingredients of this product
- more than one patch at a time
- on wounds or damaged skin
- with a heating pad
- if pouch is damaged or opened
When using this product
- avoid contact with the eyes, mucous membranes or rashes
- use only as directed
- do not bandage tightly
- do not reuse patch
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Directions
Adults and children 12 years of age and over:
- clean and dry affected area
- remove film from patch and apply to the skin (see illustration)
- apply to affected area not more than 3 to 4 times daily
- remove patch from the skin after at most 8-hour application
Children under 12 years of age: consult a doctor
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
LIDO KING ®
NDC# 73354-1280-2
MAXIMUM
STRENGTH*
LIDOCAINE 4%
Pain Relieving Gel-Patch
Apply for 8 Hours
Designed in USA
Numbing Relief
Good Skin Feel
Unscented
For temporary relief of pain
• Back
• Neck
• Shoulders
• Knees
• Elbows
• Legs
• Arms
5 PATCHES
3 15/16" x 5 1/2" (10 cm x 14 cm)
For Galaxy Bio, Inc.
Cranbury, NJ 08512
Made in China
* Available without a prescription
®Registered Trademark of NAL Pharma
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INGREDIENTS AND APPEARANCE
LIDO KING LIDOCAINE 4% PAIN RELIEVING GEL-PATCH
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73354-1280 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 POVIDONE K90 (UNII: RDH86HJV5Z) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) KAOLIN (UNII: 24H4NWX5CO) METHYLPARABEN (UNII: A2I8C7HI9T) POLYACRYLIC ACID (450000 MW) (UNII: KD3S7H73D3) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) TARTARIC ACID (UNII: W4888I119H) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) POLYSORBATE 80 (UNII: 6OZP39ZG8H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73354-1280-2 5 in 1 CARTON 11/11/2024 1 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 11/11/2024 Labeler - Galaxy Bio, Inc. (782793231)