KINGLY 4% LIDOCAINE PATCHES- 4% lidocaine patch

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine 4%

PURPOSE

Topical analgesic

INDICATIONS & USAGE

For temporary relief of pain

WARNINGS

For external use only

DO NOT USE

more than 1 patch at a time
on wounds or damaged skin with a heating pad
if you have ever had an allergic reaction to this product or any of its ingredients

WHEN USING

use only as directed

avoid contact with the eyes, mucous membranes or rashes

do not bandage tightly

STOP USE

localized skin reactions occur, such as rash, itching, redness, irritation, pain swelling and blistering
conditions worsen
symptoms persist for more than 7 days
symptoms clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

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 1 patch at a time to affected area, not more than 3 to 4 times daily

remove patch from the skin after at most 8 hours of application

Children under 12 years of age: consult a doctor

INACTIVE INGREDIENT

Aluminum Glycinate
Disodium EDTA
Ethylhexylglycerin
Glycerin
Phenoxyethanol
Polyvinyl pyrrolidone
Polysorbate 80
Sodium carboxymethyl cellulose
Sodium polyacrylate
Sorbitol
Tartaric Acid
Titanium Dioxide
Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KINGLY 4% LIDOCAINE PATCHES 
4% lidocaine patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87394-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg

Inactive Ingredients
Ingredient Name	Strength
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PVP (UNII: FZ989GH94E)
TARTARIC ACID (UNII: W4888I119H)
GLYCERIN (UNII: PDC6A3C0OX)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALUMINUM GLYCINATE (UNII: 1K713C615K)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SORBITOL (UNII: 506T60A25R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87394-002-01	40 in 1 BOX	04/13/2026
1		1 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	04/13/2026

Labeler - Shenzhen Huayuan Hengsheng Technology Co., Ltd. (570254468)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Huayuan Hengsheng Technology Co., Ltd.		570254468	manufacture(87394-002)