EQUATE HEMORRHOID RELIEF- lidocain 5% cream 
WALMART, INC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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EQUATE HEMORRHOID RELIEF CREAM- LIDOCAINE 5%

ACTIVE INGREDIENT

Lidocaine 5% W/W

PURPOSE

Local Anesthetic

USES

helps relieve the pain, itching, and burning, associated with hemorrhoids and anorectal disorders.

WARNINGS

For external use only

When using this product

  • use only as directed
  • avoid contact with eyes
  • do not exceed recommended dosage unless directed by a doctor
  • do not put this product into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

  • rectal bleeding occurs
  • condition worsens or does not improve within 7 days
  • symptoms clear up and occur again within a few days
  • an allergic reaction develops to ingredients in this product
  • symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children and pets.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

DIRECTIONS

Adult and children 12 years and over:

children under 12 years of age: consult a doctor.

OTHER INFORMATION

Store between 15°-30° C (59°-30° F)

INACTIVE INGREDIENTS

Benzyl Alcohol, Carbomer 940, Cholesterol, Isopropyl Myristate, Lecithin (Soya), Polysorbate 80, Propylene Glycol, Purified Water, Triethanolamine, Vitamin-E Acetate

QUESTIONS

1-888-287-1915

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

EQUATE HEMORRHOID RELIEF 
lidocain 5% cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-109
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
TROLAMINE (UNII: 9O3K93S3TK)  
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-109-301 in 1 CARTON04/01/2022
130 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34604/01/2022
Labeler - WALMART, INC (051957769)
Registrant - GURUNANDA, LLC (079671169)

Revised: 8/2022
Document Id: e78fd57d-3f94-d939-e053-2995a90ae4e9
Set id: d96e8152-e36e-22fc-e053-2995a90a8b2b
Version: 3
Effective Time: 20220831
 
WALMART, INC