WALMART- pyrithione zinc lotion/shampoo

Walmart by

Drug Labeling and Warnings

Walmart by is a Otc medication manufactured, distributed, or labeled by Wal-Mart Stores, Inc, Apollo Health and Beauty Care Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Pyrithione Zinc

PURPOSE

For the relief of itching, redness and flaking associated with dandruff

WARNINGS

For External use

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor ifcondition worsens or does not improve after regular use of this product.

Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

DOSAGE & ADMINISTRATION

• Adults and children 2 years and older.
• Shake well.
• Apply evenly to scalp. leave on for several minutes and then rinse off.
• Use at least twice per week or as directed by a doctor or pharmacist.

INACTIVE INGREDIENT

Water, Stearyl Alcohol, Behentrimonium Chloride, Cetyl Alcohol, Cocos Nucifera (Coconut) Oil,
Dimethicone, Fragrance, PPG-3 Benzyl Ether Ethylhexanoate, Lauryl PEG/PPG-18/18 Methicone,
Hydroxyethylcellulose, Sodium Hydroxide, Citric Acid, Methylchloroisothiazolinone,
Methylisothiazolinone.

STORAGE AND HANDLING

Store at room temperature

INDICATIONS & USAGE

Relieves itching , redness and flakes associated with Dandruff.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALMART 
pyrithione zinc lotion/shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-899
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	300 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)
CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PPG-3 BENZYL ETHER ETHYLHEXANOATE (UNII: 3N703GY99W)
WATER (UNII: 059QF0KO0R)
CETYL ALCOHOL (UNII: 936JST6JCN)
COCONUT OIL (UNII: Q9L0O73W7L)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-899-70	700 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/04/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	11/04/2022

Labeler - Wal-Mart Stores, Inc (051957769)

Registrant - Apollo Health and Beauty Care Inc. (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
Apollo Health and Beauty Care Inc.		201901209	manufacture(79903-899)