Bite And Sting Medicated Relief Pads
FDA Label NDC 69842-856

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 Medicated Relief Pads (NDC 69842-856). 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                   purpose, uses, warningsfor external use only, when using this product, stop use and ask a doctor if, direction, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient                   Purpose

Benzocaine - 5.00%                Pain Relief

Uses

For temporarily relief of pain and itching associated with minor cuts, scrapes and minor burns

Warningsfor External Use Only

Flammable: ​ do not use while smoking or near heat or flame

When Using This Product

  • avoid contact with eyes
  • use only as directed

Stop Use And Ask A Doctor If

• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

Direction

• adults and children 2 years of age and older: Apply to affected area, not more than 3 to 4 times daily
• children under 2 years of age: Ask a doctor

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Ascorbic Acid, Camphor, Chamomilla Recutita (Matricaria) Flower Extract, Cholecalciferol, Diisopropyl Adipate,
Eugenia Caryophyllus (Clove) Flower Oil, Fragrance, Mentha Piperita (Peppermint) Oil, Octyldodecanol, Olea Europaea (Olive) Fruit Oil,
PEG-8 Dimethicone, Propylene Glycol, Pyridoxine HCl, Retinyl Palmitate, SD Alcohol 40, Silica, Sodium Propoxyhydroxypropyl Thiosulfate Silica,
Tocopheryl Acetate, Zea Mays (Corn) Oil

* Please review the disclaimer below.