Waxrx Earacherx Pain Relieving Drops Liquid
FDA Label NDC 72724-002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Doctor Easy Medical Products, Llc for the product Waxrx Earacherx Pain Relieving Drops (NDC 72724-002). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, easy to use directions, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Otc - Active Ingredient

→ Otc - Purpose

→ Indications & Usage

→ Warnings

→ Otc - Stop Use

→ Otc - Keep Out Of Reach Of Children

→ Easy To Use Directions

→ Inactive Ingredient

→ Package Label.principal Display Panel

Otc - Active Ingredient

Lidocaine HCL 4%

Otc - Purpose

Lidocaine HCL 4%...................Topical Anesthetic

Indications & Usage

For the temporary relief of pain.

Warnings

Keep out of reach of children, with cap securely closed.
For external use only.
If swallowed, immediately call Poison Control 800-222-1222
Avoid contact with the eyes.
If irritation occurs, stop and seek medical advice

Otc - Stop Use

DO NOT Use

In large quantities, particularly over raw surfaces or blistered areas.
If you are allergic to any ingredient in this product.
If you have an injury or perforation (hole) of the eardrum or tubes in the ear.
If you are running a fever, or notice a discharge.
If conditions worsen, or if symptoms persist for more than 7 days, or clear up and occur again within a few days, discontinue use of this product and consult a physician.