HEMRID ANORECTAL CREAM- lidocaine cream

HemRid Anorectal Cream by

Drug Labeling and Warnings

HemRid Anorectal Cream by is a Otc medication manufactured, distributed, or labeled by KKA & Associates LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INACTIVE INGREDIENT

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

ACTIVE INGREDIENT

Lidocaine 5% W/W

PURPOSE

Local Anesthetic

DOSAGE & ADMINISTRATION

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.
To use with finger cot. Roll one finger cot over finger. Gently squeeze cream onto finger
Smooth a layer of the cream over the affected area.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away.

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 out 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.

INDICATIONS & USAGE

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HEMRID ANORECTAL CREAM 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82620-001
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
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL CALCIUM SUCCINATE, DL- (UNII: H5A1374A6R)
CHOLESTEROL (UNII: 97C5T2UQ7J)
WATER (UNII: 059QF0KO0R)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CARBOMER 940 (UNII: 4Q93RCW27E)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82620-001-01	1 in 1 CARTON	04/04/2022
1		28.3 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	04/04/2022

Labeler - KKA & Associates LLC (050979549)