San-e-foam
FDA Label NDC 61924-107

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dermarite Industries Llc for the product San-e-foam (NDC 61924-107). 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:, warnings:, otc - keep out of reach of children, directions, other information, san-e-foam package label principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient:

Ethyl Alcohol 67%

Purpose:

Antiseptic

Uses:

  • For handwashing to decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings:

For external use only.

Flammable. Keep away from heat or flame.

Avoid contact with eyes. In case of contact, flush thoroughly with water.

Stop use and ask a doctor if skin irritation develops.

Otc - Keep Out Of Reach Of Children

In case of accidental ingestion contact a physician or Poison Control Center right away.

Directions

  • Wet hands thoroughly with product.
  • Briskly rub hands until dry.
  • Supervise children in the use of this product.

Other Information

  • Do not store above 105°F. May discolor some fabrics or surfaces.
  • May report serious adverse events to DermaRite Industries, PO Box 7209, North Bergen, NJ 07047

* Please review the disclaimer below.