Bite And Sting Relief Wipe
FDA Label NDC 69842-190

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cvs for the product Bite And Sting Relief Wipe (NDC 69842-190). 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 ingredients, purpose, uses, warnings, keep out of reach of children, directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Ethyl Alcohol 50.0%

Lidocaine HCL 2.0%

Purpose

First Aid Antiseptic
Topical Analgesic

Uses

  • First aid to help guard against skin infection and temporary relief of pain and itching assocaiated with insect bites.

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

  • in the eyes over large areas of the body or bandage. 
  • in large quantities particularly over raw surfaces or blistered areas.
    • Stop use and contact a doctor if the condition persists or worsens for more than 7 days or clears up and occurs again within a few days.

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.

Directions

Adults and children 2 years and older: Apply to clean affected area no more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

Inactive Ingredients

Benzalkonium Chloride, Menthol, Water.

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