RITE AID DANDRUFF 2 IN 1 CLASSIC CLEAN- pyrithione zinc shampoo 
Rite Aid Corporation

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.

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Drug Facts - Back Label

Active Ingredient

Pyrithione Zinc 1%

Purpose

Anti-dandruff

Uses

Helps 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 with water thoroughly

Stop use and ask doctor if

Conditions worsens or 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

Inactive Ingredients

Water, Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamide MEA, Glycol Distearate, Dimethicone, Zinc Carbonate, Fragrance, Cetyl Alcohol, Polyquaternium-10, Magnesium Sulfate, Sodium Benzoate, Magnesium Carbonate Hydroxide, Ammonium Laureth Sulfate, Benzyl Alcohol, Sodium Chloride, Elaeis Guineensis (Palm) Oil, Sodium Xylenesulfonate, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 10, Blue 1, Red 4

Principle Display Panel

Rite Aid Dandruff classic clean

Large Size

Compare to Head and Shoulder®

2 in 1 Classic Clean

Dandruff Shampoo plus Conditioner

For normal or dry hair

15.2 FL OZ (449 mL)

ra.jpg15.2 OZ Front and Back Labels

RITE AID DANDRUFF  2 IN 1 CLASSIC CLEAN
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-4101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Pyrithione Zinc (UNII: R953O2RHZ5) (Pyrithione Zinc - UNII:R953O2RHZ5) Pyrithione Zinc1 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ZINC CARBONATE (UNII: EQR32Y7H0M)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ALMAGATE (UNII: 568Z59H7ZJ)  
AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PALM OIL (UNII: 5QUO05548Z)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-4101-5449 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H10/20/2010
Labeler - Rite Aid Corporation (014578892)
Registrant - Apollo Health and Beauty Care (201901209)
Establishment
NameAddressID/FEIBusiness Operations
Apollo Health and Beauty Care201901209manufacture

Revised: 10/2010
Document Id: 324f90ad-2a4b-4757-b616-aa233856d205
Set id: 40f35637-c50a-4a26-8185-db4c942b546a
Version: 1
Effective Time: 20101020
 
Rite Aid Corporation