SIGNATURE PAIN RELIEF CREAM- 4% lidocaine cream

Drug Labeling and Warnings

Drug Details [pdf]

WARNINGS

For external use only.
Do not use in large quantities, particularly over raw
surfaces or blistered areas.
When using this product, avoid contact with eyes.
Stop use and ask a doctor if the condition worsens,
symptoms persist for more than 7 days, or clear up
and occur again within a few days.

PURPOSE

External Analgesic

STOP USE

if the condition worsens,
symptoms persist for more than 7 days, or clear up
and occur again within a few days.

ACTIVE INGREDIENT

4% Lidocaine

WHEN USING

The indications for Mol are strictly for the temporary reliet of pain and itching associated with:
Minor burns and sunburns.
Minor cuts and scrapes.
Insect bites.
Minor skin irritation.

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

Adults and children 2 years of age and older: Apply to the affected area not more than
3 to 4 time daily.
Chindren under 2 years of age: Consult a doctor

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of
children.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SIGNATURE PAIN RELIEF CREAM 
4% lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84019-044
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 1 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84019-044-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/13/2026

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

Establishment
Name	Address	ID/FEI	Business Operations
Shengnan (Guangzhou) Cosmetics Co., LTD		541200425	manufacture(84019-044)