SIGNATURE LIDOCAINE PAIN RELIEF CREAM- 5% lidocaine cream

Signature Lidocaine Pain Relief Cream by

Drug Labeling and Warnings

Signature Lidocaine Pain Relief Cream by is a Otc medication manufactured, distributed, or labeled by Shengnan (Guangzhou) Cosmetics Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

For external use only.
Avoid contact with eyes.
Patch test before full use.
Discontinue use if irritation occurs.
Keep out of reach of children.

PURPOSE

Anorectal (Hemorrhoidal)

STOP USE

Allergic reaction or
rectal bleeding occurs.
Redness, irritation,
swelling, or pain increases.
Condition worsens or
lasts >7 days

ACTIVE INGREDIENT

5% Lidocaine

WHEN USING

Temporary relief of pain,itching, soreness, or burning in the perianal area from anorectal disorders.

INACTIVE INGREDIENT

Benzyl Alcohol, Carbomer 934, Lecithin (Soybean), Mentha Arvensis Leaf Extract, Chrysanthemum Indicum Extract, Portulaca Oleracea Extract,
Propylene Glycol, Tocopheryl Acetate, Water

DOSAGE & ADMINISTRATION

Adults and children 12
years and older: Apply a
thin layer to the affected
area 1-3 times daily or
as directed by a
healthcare provider.

INDICATIONS & USAGE

Wash the area with soap. Apply a 2 mm-thick layer, rub it in for 1–2 minutes, and cover with a waterproof
film approximately 90 minutes before your procedure. Scan the QR code for detailed directions.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of
children.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SIGNATURE LIDOCAINE PAIN RELIEF CREAM 
5% lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84019-043
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
CARBOMER 934 (UNII: Z135WT9208)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84019-043-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	03/06/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	03/06/2026

Labeler - Shengnan (Guangzhou) Cosmetics Co., LTD (541200425)

Establishment
Name	Address	ID/FEI	Business Operations
Shengnan (Guangzhou) Cosmetics Co., LTD		541200425	manufacture(84019-043)