Sting Relief Pad Liquid
FDA Label NDC 59050-706

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Changzhou Maokang Medical Products Co., Ltd for the product Sting Relief Pad (NDC 59050-706). 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 facts, active ingredient, purpose, directions, dosage & administration, do not use, stop use, cautionflammable , keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Benzocaine, 6% w/v

Isopropyl Alcohol 60% w/v

Purpose

Topical Anesthetic

Antiseptic

Dosage & Administration

For adults and children 2 years of age and older. Children under 2 years; consult physician.

Do Not Use

  • In the eyes. If contact occurs, rinse thoroughly with water

Stop Use

If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Cautionflammable , Keep Out Of Reach Of Children.

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

Inactive Ingredient

Purified Water

Package Labeling:

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