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Medically reviewed on May 7, 2018

Dosage form: lotion/shampoo
Ingredients: PYRITHIONE ZINC 1.2g in 1mL
Labeler: The Village Company
NDC Code: 69752-121

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.

Tegrin BACK LABEL 2in1


Naturally soothes and moisturizes while treating the symptons of dandruff.


Keep this and all drugs out of the reach of children. If swallowed, get medical help or contact a poison control center right away.


Helps prevent recurrence of flaking and itching associated with dandruff.


For external use only.

When using this product

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

Stop using and ask a doctor

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

Keep this and all drugs our of the reach of children

  • If swallowed, get medical help or contact a poison control center right away.

  • shake before use
  • wet hair, apply onto scalp, rinse, repeat if desired
  • for maximum dandruff control use every time you shampoo
  • for best results use at least twice per week or as directed by a doctor

Inactive ingredients

Water, propelyne glycol, sodum laurly sulfate, sodium laureth sulfate, cocamidopropyl betain, polyquaternium-10, polyquaternium-39, melaleuca alternifolia (tea tree) leaf oil,nigella sativa seed oil, daucus carota sativa (carrot) seed oil, salvia hispzanica seed oil, rubus idaeus (raspberry) seed oil, vaccinium macrocarpon (cranberry) seed oil, rubus occidentalis seed oil, acrylates/c10-30 alkyl acrylate crosspolymer, sodium hydroxide, methlychloroisothiazoline, methylisothiazolinone, fragrance.

Front Label

pyrithione zinc lotion/shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69752-121
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
WATER1 g  in 1 mL
Product Characteristics
Colorwhite (opaque viscous liquid) Score    
FlavorImprint Code
#Item CodePackage Description
1NDC:69752-121-14414 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H07/01/2015
Labeler - The Village Company (172208105)
Registrant - Apex International (015226132)
Apex International015226132manufacture(69752-121)

The Village Company

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.