Active Ingredient(S)
Benzocaine (7.5%)
A And E Marathon Delay Serum Cream
FDA Label NDC 87068-181
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Phe Inc for the product A And E Marathon Delay Serum (NDC 87068-181). 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 active ingredient(s), purpose, use, warnings, otc - keep out of reach of children, 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
Desensitizer
Use
Reduce sexual over-sensitivity in men.
Warnings
Methemoglobinemia warning: Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops: ■ pale, gray, or blue colored skin (cyanosis) ■ headache ■ rapid heart rate ■ shortness of breath ■ dizziness or lightheadedness ■ fatigue or lack of energy
Otc - Keep Out Of Reach Of Children
Keep out of reach of childeren. Contact a Poison Control Center: This is the emergency contact for accidental overdose or ingestion
Directions
■ Apply a small amount to the head and shaft of the penis ■ 2-3 minutes before sex. ■ For adults only. Not for sale to minors.
Other Information
Store at 20-25°C (68-77°F)
Inactive Ingredients
Water, Alcohol, Propanediol, Carbomer, PEG-40 Hydrogenated Castor Oil, PPG-26-Buteth-26, Menthyl Lactate, Potassium Sorbate, Sodium Benzoate, Sodium Hydroxide, Panthenol, Panax Ginseng Root Extract
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