HEAD AND SHOULDERS CHARCOAL DAILY- pyrithione zinc lotion/shampoo

Head and Shoulders Charcoal Daily by

Drug Labeling and Warnings

Head and Shoulders Charcoal Daily by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

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 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 this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

Inactive ingredients

Water, sodium laureth sulfate, sodium xylenesulfonate, zinc carbonate, glycol distearate, sodiumlauryl sulfate, fragrance, cocamidopropyl betaine, cocamide MEA, dimethicone, menthol, guar hydroxypropyltrimonium chloride, sodiumbenzoate, sodium chloride, stearyl alcohol, magnesiumcarbonate hydroxide, cetyl alcohol, polyquaternium-76, methylchloroisothiazolinone, methylisothiazolinone, charcoal extract, yellow 5, red 33, blue 1.

Questions (or comments)?

1-800-723-9569

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 650 mL Bottle Label

head &
shoulders ®

pyrithione zinc dandruff shampoo

CHARCOAL

DAILY SHAMPOO

DEEPLY PURIFIES AND REMOVES

IMPURITIES FROM SCALP AND HAIR

21.9 FL OZ

(650 mL)

INGREDIENTS AND APPEARANCE

HEAD AND SHOULDERS CHARCOAL DAILY 
pyrithione zinc lotion/shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-278
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 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
CETYL ALCOHOL (UNII: 936JST6JCN)
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
ZINC CARBONATE (UNII: EQR32Y7H0M)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
DIMETHICONE (UNII: 92RU3N3Y1O)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-278-38	380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/15/2018
2	NDC: 69423-278-65	650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/15/2018	12/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	11/15/2018

Labeler - The Procter & Gamble Manufacturing Company (004238200)