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Zincon Medicated Dandruff by Neoteric Cosmetics, Inc.

Dosage form: shampoo
Ingredients: PYRITHIONE ZINC 0.01g in 1mL
Labeler: Neoteric Cosmetics, Inc.
NDC Code: 62673-016

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Zincon Medicated Dandruff Shampoo

Active Ingredient

Pyrithione zinc 1%

Purpose

Anti-dandruff

Uses
  • reduces and helps eliminate scalp itching, flaking and scaling associated with dandruff and seborrheic dermatitis. 

Warnings

For external use only.

Ask a doctor before use if you have

a condition that covers a large area of the body.

When using this product

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

Stop use and ask a doctor if
  • condition worsens
  • condition does not improve after regular use of this product as directed.

Keep out of reach of children.

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

Directions
  • shake well
  • wet hair, apply to scalp and massage vigorously
  • rinse and repeat
  • 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

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.

Questions?

1-800-220-0151

www.denorex.net

PRINCIPAL DISPLAY PANEL

Pyrithione Zinc
Zincon®
MEDICATED
 
DANDRUFF SHAMPOO

8 fl.oz. (118ml)

ZINCON MEDICATED DANDRUFF 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62673-016
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC0.01 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE 
COCO MONOETHANOLAMIDE 
WATER 
FD&C BLUE NO. 1 
GLYCOL DISTEARATE 
MAGNESIUM ALUMINUM SILICATE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
PROPYLENE GLYCOL 
SODIUM CHLORIDE 
SODIUM LAURETH SULFATE 
SODIUM LAURYL SULFATE 
Packaging
#Item CodePackage Description
1NDC:62673-016-94118 mL in 1 BOTTLE
2NDC:62673-016-98236 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H12/13/2017
Labeler - Neoteric Cosmetics, Inc. (790615181)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIOperations
Humco Holding Group, Inc.825672884manufacture(62673-016), analysis(62673-016), pack(62673-016), label(62673-016)

 
Neoteric Cosmetics, Inc.

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Medically reviewed on Dec 13, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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