FDA.reportPublic FDA data

Zincon Medicated Anti-Dandruff

Manufacturer
Neoteric Cosmetics, Inc.
Effective date
2025-01-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:01:54

Label at a glance#

ProductZincon Medicated Anti-Dandruff
Active ingredientPYRITHIONE ZINC
Label structure10 sections

Indications and uses

Reduces and helps eliminate scalp itching, flaking and scaling associated with dandruff and seborrheic dermatitis.

Dosage and administration

Shake well Wet hair, apply shampoo and work into lather Rinse thoroughly For best results, use at least twice a week or as directed by a doctor Do not use on children under 2 years of age, except as directed by a doctor

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione zinc 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

Reduces and helps eliminate scalp itching, flaking and scaling associated with dandruff and seborrheic dermatitis.

Warnings:

WARNINGS SECTION

For external use only.

Ask a doctor before use if you

OTC - ASK DOCTOR SECTION

have a condition that covers a large area of the body.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

condition worsens or does not improve after regular use of this product as directed.

Keep out of reach of children:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Shake well
  • Wet hair, apply shampoo and work into lather
  • Rinse thoroughly
  • For best results, use at least twice a week or as directed by a doctor
  • Do not use on children under 2 years of age, except as directed by a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water/Eau, Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Cocamide MEA, Glycol Distearate, Glycerin, Propylene Glycol, Sodium Chloride, Magnesium Aluminum Silicate, Magnesium Nitrate, Sodium Polynaphthalenesulfonate, Xanthan gum, Citric Acid, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone, Fragrance/Parfum, CI 42090 (Blue 1)

Questions?

OTC - QUESTIONS SECTION

Call 1-877-524-8306

email info@zincon.com or visit www.zincon.com

SPL UNCLASSIFIED SECTION

Zincon® MEDICATED

ANTI-DANDRUFF SHAMPOO

PYRITHIONE ZINC 1%

Distributed by Neoteric Cosmetics, Inc.

New York 10003 / Made in Canada

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZINCON®
MEDICATED
ANTI-DANDRUFF SHAMPOO

Pyrithione Zinc 1%

DAILY CONTROL OF DANDRUFF, FLAKING, ITCHING & IRRITATION

LEAVES HAIR CLEAN & EASY TO MANAGE

REFRESHING, CLEAN SCENT

8 fl.oz. (236 ml)

labellabel

drug factsdrug facts

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN2
1246250Zincon Dandruff 1 % Medicated ShampooPSN2
1246250zinc pyrithione 10 MG/ML Medicated Shampoo [Zincon]SBD2
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD2
209884zinc pyrithione 1 % Medicated ConditionerSY2
209884zinc pyrithione 1 % Medicated ShampooSY2
1246250Zincon 10 MG/ML Medicated ShampooSY2
1246250Zincon Dandruff 1 % Medicated ShampooSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62673-017-94Zincon Medicated Anti-Dandruff118 mL in 1 BOTTLESHAMPOO1182
62673-017-98Zincon Medicated Anti-Dandruff236 mL in 1 BOTTLESHAMPOO2362

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62673-01762673-017-94, 62673-017-98

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
FORMALDEHYDE/SODIUM NAPHTHALENESULFONATE COPOLYMER (3000 MW)90D834OZUIIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
XANTHAN GUMTTV12P4NEEIACT
MAGNESIUM NITRATE77CBG3UN78IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
COCO MONOETHANOLAMIDEC80684146DIACT
WATER059QF0KO0RIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
GLYCOL DISTEARATE13W7MDN21WIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM LAURYL SULFATE368GB5141JIACT
PYRITHIONE ZINCR953O2RHZ5ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Zincon Medicated Anti-DandruffPYRITHIONE ZINCNeoteric Cosmetics, Inc.2c26bd1e-35d4-f1a2-e063-6294a90af5762025-01-23WarningsExact identifier
ndc (package): 62673-017-98
ndc (package): 62673-017-94
ndc (product): 62673-017
ndc11 (package): 62673001794
ndc11 (package): 62673001798
spl id: 2c620236-34dd-7a1a-e063-6394a90a0a72
spl set id: 2c26bd1e-35d4-f1a2-e063-6294a90af576

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.