EQUATE HEMORRHOID RELIEF- lidocain 5% cream

EQUATE HEMORRHOID RELIEF by

Drug Labeling and Warnings

EQUATE HEMORRHOID RELIEF by is a Otc medication manufactured, distributed, or labeled by WALMART, INC, GURUNANDA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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:

• when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.
• apply externally to the affected area up to 6 times a day

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

INGREDIENTS AND APPEARANCE

EQUATE HEMORRHOID RELIEF 
lidocain 5% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-109
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-109-30	1 in 1 CARTON	04/01/2022
1		30 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	04/01/2022

Labeler - WALMART, INC (051957769)

Registrant - GURUNANDA, LLC (079671169)