Triclotrex-b
FDA Label NDC 66854-016

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Spai-sons Pharmaceutical International Cosmetics for the product Triclotrex-b (NDC 66854-016). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, 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

THIS PRODUCT IS AN ANTIBACTERIAL GEL WHICH PRODUCES A SYNERGISTIC EFFECT BETWEEN THE TRICLOSAN IS THE ACTIVE INGREDIENT WITH A VOLATILE CARRIER SUCH AS ALCOHOL.

Otc - Purpose

THIS PRODUCT ACT AS A PROTECTOR AGAINST FUNGI AND BACTERIA.

Otc - Keep Out Of Reach Of Children

THIS PRODUCT MUST BE KEEP OUT  REACH OF EYES CHILDREN.

Indications & Usage

THIS PRODUCT IS FOR TOPICAL APPLICATION,

Warnings

IF THIS PRODUCT TO CONTACT WITH EYES RINSE IMMEDIATELY WITH WATER AND CONSULT YOUR DOCTOR

Dosage & Administration

APPLY A MODERATE AMOUNT OF TRICLOTREX GEL ON THE PALM OF YOUR HAND AND RUB SPREADING IT EVENLY OVER BOTH HANDS.

Inactive Ingredient

TRICLOSAN, CETIOL AND ALOE VERA EXTRACTS BUILT A PROTECTIVE GLOVE FOR YOUR HANDS PREVENTING THE CONTAMINATION CAUSED BY FUNGI AND BACTERIA

Package Label.Principal Display Panel

IMAGE OF THE LABEL

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