The following Structured Product Label (SPL) was submitted to the FDA by Teresa Cecena Dba Genesis for the product Head And Shoulders (NDC 69772-139). 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 warnings, indications & usage, otc - active ingredient, inactive ingredient, otc - keep out of reach of children, otc - purpose, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
WARNININGS
FOR EXTERNAL USE ONLY.
WHEN USING THIS PRODUCT
Stop use and ask a doctor if
condition worsens or does not improve after regular use of this product as directed.
DIRECTIONS
PYRITHIONE ZINC 1%
Water,sodium laureth sulfate, sodium lauryl sulfate, cocamide mea, zinc carbonate, glycol distearate, dimethicone, fragance, guarhydroxypropyltrimonium chloride, magnesium sulfate, sodium benzoate, magnesium carbonate hydroxide, ammonium laureth sulfate, sodium chloride, methylchloroisothiazolinone,methylisothiazolinone, sodium xylenesulfonate, blue 1, D&C red 33.
KEEP THIS AND ALL DRUGS OUT OF REACH OF CHILDREN
PURPOSE
Anti-drandruff
FOR EXTERNAL USE ONLY
FOR BEST RESULTS USE A LEAST TWICE A WEEK OR AS DIRECTED BY A DOCTOR
Head And Shoulder (H S)
* Please review the disclaimer below.
