HEMORRHOIDAL RELIEF CREAM- lidocaine, zinc oxide cream cream

Hemorrhoidal Relief Cream by

Drug Labeling and Warnings

Hemorrhoidal Relief Cream by is a Otc medication manufactured, distributed, or labeled by Kanamed Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine 4%

Zinc Oxide 1%

INDICATIONS & USAGE

For temporary relief of anorectal discomfort, itching pain, and soreness associated with hemorrhoids, anorectal disorders or inflamed hemorrhoidal tissue.​

INACTIVE INGREDIENT

• Hemp seed oil
• Alovera Juice
• Calendula Oil
• Bhringraja Oil
• Phenylephrine Hydrochloride
• Carbopol 940
• Cetostearyl
• Cetomacrogol 1000
• Silicon Oil 350
• Glycerine
• Propyl Glycol
• Triethanalamine
• Phenoxyethanol
• Ethylhexlglycerin
• DM Water

DOSAGE & ADMINISTRATION

Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly or by patting or blotting with an appropriate cleansing pad. 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 daily.
Children under 12 years of age: consult a doctor.

WARNINGS

If condition worsens or does not improve within 7 days, consult a doctor.
Do not exceed the recommended daily dosage unless directed by a doctor.
In case of bleeding, consult a doctor promptly.
Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PURPOSE

For temporary relief of anorectal discomfort, itching pain, and soreness associated with hemorrhoids, anorectal disorders or inflamed hemorrhoidal tissue.​​

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HEMORRHOIDAL RELIEF CREAM 
lidocaine, zinc oxide cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73239-1901
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 mg  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
HEMP (UNII: TD1MUT01Q7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73239-1901-1	50 mL in 1 TUBE; Type 0: Not a Combination Product	10/16/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/16/2019

Labeler - Kanamed Inc. (117131580)

Registrant - Kanamed Inc. (117131580)