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Dandruff by HEB

Medically reviewed on May 8, 2018

Dosage form: shampoo
Ingredients: PYRITHIONE ZINC 1mg in 1mL
Labeler: HEB
NDC Code: 37808-153

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.

Drug Facts

Claims

Dandruff Shampoo

Everyday Clean

Dandruff Care for Great Looking Hair.  Helps

relieve scalp dryness, itch, irritation and helps prevent flakes.

Acitive ingredient

Pyrithione zinc

Purpose

Anti-dandruff

Use

helps prevent recurrence of flaking and itching associated with dandruff

Warnings

For external use only

When using this product
  • do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if
  • condition worsens or does not improve after regular use as directed

Keep out of reach of children.

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

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

inactive ingredients

water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, sodium chloride, zinc carbonate, sodium xylenesulfonate, amodimethicone, cocamidopropyl betaine, fragrance, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, citric acid, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33

Questions

Call 1-888-593-0593

Adverse reactions

MADE WITH PRIDE AND CARE FOR H-E-B

SAN ANTONIO, TX 78204

153.008/153BA

Principal Display Panel

H-E-B

DANDRUFF

SHAMPOO

WITH PYRITHIONE ZINC

EVERYDAY CLEAN

FOR NORMAL HAIR

Leaves Hair

Healthy Looking &

Fights Dry Scalp

14.2 FL OZ (420 mL)

DANDRUFF 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-153
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURYL SULFATE 
SODIUM LAURETH SULFATE 
GLYCOL DISTEARATE 
SODIUM CHLORIDE 
ZINC CARBONATE 
SODIUM XYLENESULFONATE 
AMODIMETHICONE (800 CST) 
COCAMIDOPROPYL BETAINE 
SODIUM BENZOATE 
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) 
MAGNESIUM CARBONATE HYDROXIDE 
CITRIC ACID MONOHYDRATE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
FD&C BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:37808-153-15420 mL in 1 BOTTLE, PLASTIC
2NDC:37808-153-35700 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H09/26/2016
Labeler - HEB (007924756)
Registrant - Vi-Jon, Inc (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon, Inc790752542manufacture(37808-153)

 
HEB

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Further information

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

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