Antiseptic Instant Pain Relief Liquid
FDA Label NDC 82645-902

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Pharma Nobis, Llc for the product Antiseptic Instant Pain Relief (NDC 82645-902). 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:, when using this product:, stop use and consult a doctor if:, keep out of the reach of children., directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Camphor 10.8%, Phenol 4.7 %

Purpose

Pain Reliever, Antiseptic

Uses:

Helps prevent infection and temporarily relieves pain and itching in minor burns, cuts, insect bites, scrapes, sunburn and other minor skin irritations.

Warnings:

For External Use Only. Do not induce vomiting. If vomiting occurs give fluids again. Do not use in or near the eyes: In case of eye contact, flush eyes with running water for 15 minutes, get medical attention immediately. Do not use on: deep punture wounds, animal bites, serious burns.

When Using This Product:

Do not bandage. Do not use over large areas of the body.

Stop Use And Consult A Doctor If:

Condition worsens. Symptoms last more than 7 days or clear up and occur again in a few days.

Keep Out Of The Reach Of Children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions:

Adult and children 2 yrs and older: apply to affected area 1 to 3 times daily.

Children under 2 yrs of age: Consult a doctor before use.

Inactive Ingredients:

Citric acid, Eucalyptus Oil, Light Mineral Oil

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