EQUATE PAIN RELIEF CREAM- 4% lidocaine hcl liquid 
Walmart, Inc

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Equate Pain Relief Cream (Roll On)

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.

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.

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

For temporary relief of pain and itching.

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

Topical Analgesic

Lidocaine 4%

lidocaine

EQUATE PAIN RELIEF CREAM 
4% lidocaine hcl liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-634
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-634-9774 mL in 1 CONTAINER; Type 0: Not a Combination Product12/21/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/21/2018
Labeler - Walmart, Inc (051957769)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114label(49035-634) , pack(49035-634) , manufacture(49035-634) , analysis(49035-634)

Revised: 12/2023
Document Id: 0ce5731a-7e1f-654e-e063-6294a90a2b5c
Set id: 7d8e8a9a-5474-4c7b-e053-2991aa0a29f5
Version: 5
Effective Time: 20231219
 
Walmart, Inc