Drug Facts

Active Ingredient

Benzocaine 5%

Anorectal (Hemorrhoidal) Gel

For external use only.

Avoid contact with the eyes.
Certain persons can develop allergic reactions from 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.

If swallowed get medical help or contact a Poison Control Center right away.

When practial, 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 to the affected area up to 6 times daily.

Do not use if safety seal is broken or missing.

Cannabis Sativa (Hemp) Seed Oil, Hydroxyethylcellulose, Methylparaben, PEG-8, Polysorbate 20, Propylene Glycol, Propylparaben, Water.

Label

BODY ACTION PRODUCTS BUTT EZE BENZOCAINE
benzocaine gel

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	50 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:70742-286-00	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M015	04/29/2022

Labeler - PRODUCT MAX GROUP INC (134893911)