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Daylogic 2 in 1 Dandruff Classic Scent

Medically reviewed on June 15, 2018

Dosage form: shampoo
Ingredients: PYRITHIONE ZINC 10mg in 1mL
Labeler: Rite Aid Corporation
NDC Code: 11822-4332

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

Active ingredient

Pyrithione Zinc 1%

Purpose

Anti-dandruff

Uses

to help prevent recurrence of flaking and itching associated with dandruff.

Warnings

For external use only.

When using this product

avoid contact with 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 of this product as directed.

Keep out of reach out of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions
  • for maximum dandruff control, use every time you shampoo.
  • wet hair, massage onto scalp and rinse.
  • repeat if desired.

Inactive ingredients

Water (Aqua), Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Sodium Chloride, Glycol Distearate, Fragrance (Parfum), Zinc Carbonate, Sodium Xylenesulfonate, Dimethicone, Cocamidopropyl Betaine, Guar Hydroxypropyltrimonium Chloride, Magnesium Carbonate Hydroxide, Sodium Benzoate, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).

Label Copy

DAYLOGIC 2 IN 1 DANDRUFF  CLASSIC SCENT
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-4332
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURYL SULFATE 
SODIUM LAURETH SULFATE 
SODIUM CHLORIDE 
GLYCOL DISTEARATE 
ZINC CARBONATE 
SODIUM XYLENESULFONATE 
DIMETHICONE 
COCAMIDOPROPYL BETAINE 
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) 
MAGNESIUM CARBONATE HYDROXIDE 
SODIUM BENZOATE 
CITRIC ACID ACETATE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
FD&C BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:11822-4332-3701 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H06/14/2016
Labeler - Rite Aid Corporation (014578892)
Registrant - Apollo Health and Beauty Care (201901209)
Establishment
NameAddressID/FEIOperations
Apollo Health and Beauty Care201901209manufacture(11822-4332)

 
Rite Aid Corporation

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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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