EQUATE PAIN RELIEF CREAM- 4% lidocaine hcl liquid

Equate Pain Relief Cream by

Drug Labeling and Warnings

Equate Pain Relief Cream by is a Otc medication manufactured, distributed, or labeled by Walmart, Inc, Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Adults and children 2 yrs of age and older: apply to the affected area no more than 3 to 4 times daily.

Children under 2 years of age: consult a doctor.

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

do not apply to wounds or damaged skin

do not use in large quantities, particularly over raw surfaces or blistered areas.

INACTIVE INGREDIENT

actylates/C10-C30 Alkyl Acrylate Crosspolymer

Aloe Barbadensis Leaf Etract

Aminoethyl Propanol

C30-C40 Alkyl Cetearyl Dimethicone Crosspolymer

Caprylyl Methicone

Cetearyl Alcohol

Ceteth-20 Phosphate

Dicetyl Phosphate

Dimethicone

Disodium EDTA

Ethylhexylglycerin

Glyceryl Stearate

Methylparaben

SD Alcohol 40

Steareth021

Purified water

INDICATIONS & USAGE

For temporary relief of pain and itching.

KEEP OUT OF REACH OF CHILDREN

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

PURPOSE

Topical Analgesic

ACTIVE INGREDIENT

Lidocaine 4%

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EQUATE PAIN RELIEF CREAM 
4% lidocaine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-634
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	4 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
METHYLPARABEN (UNII: A2I8C7HI9T)
STEARETH-21 (UNII: 53J3F32P58)
WATER (UNII: 059QF0KO0R)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
DISODIUM HEDTA (UNII: KME849MC7A)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIMETHICONE (UNII: 92RU3N3Y1O)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
CETEARYL PHOSPHATE (UNII: 4O6GCK4CTJ)
CETETH-20 PHOSPHATE (UNII: 921FTA1500)
(C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
C30-45 ALKYL METHICONE (UNII: NFX970DSI2)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49035-634-97	74 mL in 1 CONTAINER; Type 0: Not a Combination Product	12/21/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	12/21/2018

Labeler - Walmart, Inc (051957769)

Registrant - Humco Holding Group, Inc (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc		825672884	label(49035-634) , pack(49035-634) , manufacture(49035-634) , analysis(49035-634)