Drug Factsactive Ingredient
Benzocaine 5%
Ez Access
FDA Label NDC 70742-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Product Max Group Inc for the product Ez Access (NDC 70742-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug factsactive ingredient, purpose, keep out of reach of children, uses, warnings, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
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