Stingeze
FDA Label NDC 68093-7038

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Wisconsin Pharmacal Company for the product Stingeze (NDC 68093-7038). 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, purpose, uses, warnings, when using this product, stop use and ask doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredients                                                         Purpose

Benzocaine 5%...........................................................................Analgesic, Anesthetic, Antipuritic

Phenol 1.35%.............................................................................First Aid Antiseptic

Camphor 3.0%............................................................................External Analgesic

Purpose

Analgesic, Anesthetic, Antipuritic

First Aid Antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes, and burns.

Warnings

For external use only.

When Using This Product

  • Do not get in eyes
  • Do not apply over large areas of the body
  • In case of deep or puncture wounds, animal bites, or serious burns consult a doctor
  • Do not bandage.

Stop Use And Ask Doctor If

condition worsens, or symptoms persist for more than 7 days or clear up and occur again within a few days.  Do not use longer than one week unless directed by a doctor.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a poison control center right away.  If in eyes, flush with water for 15 minutes and call a physician.

Directions

  • Clean area
  • Apply a small amount to the bite area while massaging with sponge tip applicator.  If itching persists, apply again in 10-15 minutes
  • For ticks and bees, remove tick or stinger before treatment
  • Adults and children 2 years and over: Apply to affected area 1 to 3 times daily
  • Children under 2 years: Consult a doctor

Inactive Ingredients

Propylene Glycol

Questions Or Comments?

1-800-558-6614

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Bottle Label (C3310b)

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Carton Label (D3310b)

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