Active Ingredients
DIDECYLDIMONIUM CHLORIDE
BENZALKONIUM CHLORIDE
Sterite Neutrum
FDA Label NDC 81576-3000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Palvi Mexico, S.a. De C.v. for the product Sterite Neutrum (NDC 81576-3000). 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, indications and usage, dosage and administration, warnings, warnings and precautions section, keep out of reach of children, stop use section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
PURPOSE
ANTIMICROBIAL
Indications And Usage
USES
HAND AND SURFACE DISINFECTANT TO HELP REDUCE BACTERIA THAT POTENTIALLY CAUSE DISEASES
Dosage And Administration
DIRECTIONS SPRAY STERITE NEUTRUM ON 12 TO 16 INCHES OVER HANDS, RUB AND AIR DRY, ON SURFACES APPLYING A FINE MIST, WIPE CLEAN. NO RINSING REQUIRED.
Warnings
WARNING FOR EXTERNAL USE ONLY
Warnings And Precautions Section
DO NOT USE ON OPEN WOUNDS ON THE SKIN, EYES OR MUCOUS MEMBRANES
DO NOT USE IN EYES. IF CONTACT OCCURS, FLUSH THE EYES WELL WITH PLENTY OF WATER.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Stop Use Section
STOP USE AND SEE A DOCTOR IF IRRITATION OR RASH OCCURS
THESE COULD BE SIGNS OF A SERIOUS CONDITION
Inactive Ingredient Section
INACTIVE INGREDIENTS: WATER, N-NONYLPHENOL, EUCALYPTOL, DISODIUM EDTA,
* Please review the disclaimer below.
