Sanifoam Hand Sanitizer
FDA Label NDC 50536-039

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by American Chemical And Sanitary Supply Inc for the product Sanifoam Hand Sanitizer (NDC 50536-039). 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 otc - active ingredient, otc - purpose, warnings, indications & usage, otc - keep out of reach of children, inactive ingredient, dosage & administration, 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

Otc - Active Ingredient

ACTIVE INGREDIENT:

ALCOHOL (62% V/V)

Otc - Purpose

PURPOSE:

ANTIMICROBIAL

Warnings

FIRST AID:

EYES: AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER. CALL PHYSICIAN IF IRRITATION OR REDNESS DEVELOPS AND LASTS.

INGESTION: IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL OR CONTACT A POISON CNTROL CENTER IMMEDIATELY.

CONTAINER DISPOSAL: RINSE THREE TIMES WITH WATER. THEN OFFER FOR RECYCLING OR RECONDITIONING OR PUNCTURE AND DISPOSE OF IN A SANITARY LANDFILL OR BY INCARCERATION OR, IF ALLOWED BY STATE AND LOCAL AAUTHORITIES, BY BURNING. IF BURNED, STAY AWAY FROM SMOKE.

Indications & Usage

USES: Hygienic disinfectant.

Otc - Keep Out Of Reach Of Children

FOR USE BY SERVICE PROFESSIONALS ONLY.

KEEP OUT OF REACH OF CHILDREN.

Inactive Ingredient

INACTIVE INGREDIENTS: WATER

Dosage & Administration

DIRECTIONS:

POUR GEL INTO DISPENSER AND USE STRAIIGHT; DO NOT DILUTE. WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING. FOR EXTERNAL USE ONLY.

Package Label.Principal Display Panel

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