EZ ACCESS- benzocaine liquid

EZ ACCESS by

Drug Labeling and Warnings

EZ ACCESS by is a Otc medication manufactured, distributed, or labeled by Product Max Group Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug FactsActive Ingredient

Benzocaine 5%

Purpose

Topical Analgesic

Keep out of reach of children

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

Uses

• For temporary relief of pain or soreness in the perianal area.

Warnings

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 a consult a doctor.

Directions

• When practical, cleanse the affected area with mild soap and water and rinse thoroughly.
• Gently dry by patting or blotting with a tissue or a soft cloth before the application of this product.
• Apply to the affected area up to 6 times daily.

Other information

Do not use if safety tab is broken or missing

Inactive Ingredients

Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water

EZ ACCESS product label

Anal Desensitizer

EZ ACCESS

DESENSITIZING SPRAY
BENZOCAINE ANORECTAL SPRAY

1.0 FL OZ (30mL)

www.bodyactionproducts.com

Distributed by: BodyAction Products, Lutz, FL 33559

action BODY products

INGREDIENTS AND APPEARANCE

EZ ACCESS 
benzocaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70742-001
Route of Administration	Topical

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	1417 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70742-001-01	30 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/15/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part348	06/15/2016

Labeler - Product Max Group Inc (134893911)

Registrant - Product Max Group Inc (134893911)