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

Rite Aid Dandruff by

Drug Labeling and Warnings

Rite Aid Dandruff by is a Otc medication manufactured, distributed, or labeled by Rite Aid Corporation, Apollo Health and Beauty Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• Shake well, wet hair, massage onto scalp, rinse. Repeat if desired.
• For best results use at least twice a week or as directed by a doctor.
• For maximum dandruff control, use every time you shampoo
  

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)

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INGREDIENTS AND APPEARANCE

RITE AID DANDRUFF  2 IN 1 CLASSIC CLEAN
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-4101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Pyrithione Zinc (UNII: R953O2RHZ5) (Pyrithione Zinc - UNII:R953O2RHZ5)	Pyrithione Zinc	1 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-4101-5	449 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	10/20/2010

Labeler - Rite Aid Corporation (014578892)

Registrant - Apollo Health and Beauty Care (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
Apollo Health and Beauty Care		201901209	manufacture