Active Ingredient Section
DIDECYLDIMONIUM CHLORIDE
BENZALKONIUM CHLORIDE
Sterite Element
FDA Label NDC 81576-2000
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 Element (NDC 81576-2000). 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 section, purpose section, indications and usage section, dosage and administration section, keep out of reach of children section, warnings and precautions section, warnings section, stop use section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose Section
PURPOSE
ANTIMICROBIAL
Indications And Usage Section
USES
HAND AND SURGACE DISINFECTANT TO HELP REDUCE BACTERIA THAT POTENTIALLY CAUSE DISEASES
Dosage And Administration Section
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.
Keep Out Of Reach Of Children Section
KEEP OUT OF REACH OF CHILDREN
Warnings And Precautions Section
DO NOT USE ON OPEN WOUNDS ON THE SKIN, EYES OR MUCOUS MEMBRANES
Warnings Section
DO NOT USE IN EYES. IF CONTACT OCCURS, FLUSH THE EYES WELL WITH PLENTY OF WATER.
Stop Use Section
STOP USE AND SEE A DOCTOR IF IRRITATION OR RASH OCCURS
Inactive Ingredients
INACTIVE INGREDIENTS: WATER N-NONYLPHENOL, EUCALYPTOL, MANDARIN OIL, SODIUM BICARBONATE, DISODIUM EDTA.
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