NUMBING CREAM- lidocaine cream

Numbing Cream by

Drug Labeling and Warnings

Numbing Cream by is a Otc medication manufactured, distributed, or labeled by Everyday Medical LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Lidocaine 5% Topical Analgesic

PURPOSE

Topical analgesic

INDICATIONS & USAGE

temporarily relieves minor pain associated with

• arthritis
• simple backache
• muscle strains
• bruises
• sprains
• cramps

WARNINGS

Warnings

For external use only

When using this product: Use only as directed

• do not bandage tightly or use with a heating pad
• avoid contact with eyes and mucous membranes
• do not apply to wounds or damaged, broken or irritated skin
• if severe burning sensation occurs, discontinue use immediately

Stop use and ask a doctor if

• condition worsens
• redness is present
• irritation develops

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

• Use only as directed
• Adults and children 12 years of age and older apply a thin layer to affected area every 6 to 8 hours not to exceed 3 applications in a 24 times period
• Children under the age of 12 years of age consult a doctor

INACTIVE INGREDIENT

MELALEUCA ALTERNIFOLIA LEAF
CYCLOMETHICONE 5
PHENYL TRIMETHICONE
ALKYL (C12-15) BENZOATE
CLOVE OIL
CARBOMER INTERPOLYMER TYPE A (55000 CPS)
WATER
ALOE VERA LEAF
CETYL ALCOHOL
LICORICE
GLYCERIN
STEARIC ACID
EDETIC ACID
GLYCERYL STEARATE/PEG-100 STEARATE
SODIUM HYDROXIDE
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE
BUTYLATED HYDROXYTOLUENE
CETOSTEARYL ALCOHOL
CETEARYL GLUCOSIDE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NUMBING CREAM 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72982-1904
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
CLOVE OIL (UNII: 578389D6D0)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CETYL ALCOHOL (UNII: 936JST6JCN)
LICORICE (UNII: 61ZBX54883)
GLYCERIN (UNII: PDC6A3C0OX)
STEARIC ACID (UNII: 4ELV7Z65AP)
EDETIC ACID (UNII: 9G34HU7RV0)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72982-1904-1	120 g in 1 CONTAINER; Type 0: Not a Combination Product	07/08/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/08/2019

Labeler - Everyday Medical LLC (117001767)

Registrant - Everyday Medical LLC (117001767)