BODEWELL DRY SCALP DAILY- pyrithione zinc lotion/shampoo
The Procter & Gamble Manufacturing Company

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Bodewell Dry Scalp Daily

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, cocamide MEA, sodium xylenesulfonate, zinc carbonate, glycol distearate, sodium lauryl sulfate, sodium chloride, cocamidopropyl betaine, fragrance, dimethicone, guar hydroxypropyltrimonium chloride, sodium benzoate, hydrochloric acid, stearyl alcohol, magnesium carbonate hydroxide, cetyl alcohol, polyquaternium-76, prunus amygdalus dulcis (sweet almond) oil, methylchloroisothiazolinone, methylisothiazolinone.

Questions (or comments)?

1-800-213-1873

MADE IN U.S.A. of U.S. and/or Imported Ingredients

Dist. by THE PROCTER & GAMBLE DISTRIBUTING, LLC
CINCINNATI, OH 45202

bodewellskin.com

PRINCIPAL DISPLAY PANEL - 237 mL Bottle Label

bodewell

dry scalp

daily

shampoo

PYRITHIONE ZINC DANDRUFF

SHAMPOO

8.0 FL OZ (237mL)

BOD

BODEWELL DRY SCALP DAILY
pyrithione zinc lotion/shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69423-736
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	1 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
CETYL ALCOHOL (UNII: 936JST6JCN)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
DIMETHICONE (UNII: 92RU3N3Y1O)
ZINC CARBONATE (UNII: EQR32Y7H0M)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
HYDROCHLORIC ACID (UNII: QTT17582CB)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
ALMOND OIL (UNII: 66YXD4DKO9)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69423-736-23	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/03/2022	12/31/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M032	03/03/2022	12/31/2023

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 11/2023

Document Id: 0a22ff14-3827-3db1-e063-6394a90ab42f

Set id: 0a22fa72-c360-4e96-e063-6394a90a48aa

Version: 1

Effective Time: 20231114

The Procter & Gamble Manufacturing Company