Active Ingredient
Pyrithione zinc 1%
The following Structured Product Label (SPL) was submitted to the FDA by Neoteric Cosmetics, Inc. for the product Zincon Medicated Dandruff (NDC 62673-016). 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 active ingredient, purpose, uses, warnings, ask a doctor before use if you have, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Pyrithione zinc 1%
Anti-dandruff
For external use only.
a condition that covers a large area of the body.
avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
If swallowed, get medical help or contact a Poison Control Center right away.
Citric acid, cocamide MEA, deionized water, FD&C Blue 1, fragrance, glycol distearate, magnesium aluminum silicate, Methylchloroisothiazolinone, Methylisothiazolinone, propylene glycol, sodium chloride, sodium laureth sulfate, sodium lauryl sulfate.
1-800-220-0151
www.denorex.net
Pyrithione Zinc
Zincon®
MEDICATED
DANDRUFF SHAMPOO
8 fl.oz. (118ml)
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