Active Ingredient
Pyrithione zinc 1%
(To the right)
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, 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%
(To the right)
Anti-dandruff
have a condition that covers a large area of the body.
avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Citric acid, cocamide MEA, deionized water, FD & C Blue No. 1, Fragrance, glycol distearate, magnesium aluminum silicate, methylchloroisothiazolinone, methylisothiazolinone, propylene glycol, sodium chloride, sodium laureth sulfate, sodium lauryl sulfate.
Questions? 1-800-220-0151
Manufactured for Neoteric Cosmetics, Inc.
Denver, CO 80239
WWW. Neotericcosmetics.com MADE IN USA
Pyrithione Zinc
ZINCON
MEDICATED
DANDRUFF SHAMPOO
4 fl.oz. (118ml)
Pyrithione Zinc
ZINCON
MEDICATED
DANDRUFF SHAMPOO
8 fl.oz. (236ml)
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