WALGREENS SCALP ITCH RELIEF- hydrocortisone liquid

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Hydrocortisone 1%

PURPOSE

Anti-itch liquid

INDICATIONS & USAGE

Temporarily relieves itching associated with minor skin irritations, inflammation, and rashes due to: eczema, psoriasis, and seborrheic dermatitis. Other uses of this product should be only under the advice and supervision of a doctor.

WARNINGS

For external use only. Use only as directed.

Flammable. Keep away from fire or flame.

Do not use for the treatment of diaper rash; consult a doctor if you are allergic to any ingredient in this product.

When using this product avoid contact with eyes, do not use more than directed unless told to by a doctor.

Stop use and ask a doctor if condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, do not use this or any other hydrocortisone product unless you have asked a doctor.

PREGNANCY OR BREAST FEEDING

Ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Adults and children 2 years of age and older:

• apply to affected area not more than 3 to 4 times daily
• if applying after shampooing, towel dry hair before use
• squeeze bottle gently to avoid excess dripping
• apply solution directly to scalp and massage in
• twist applicator tip tightly after use
• children under 2 years of age: do not use, ask a doctor

INACTIVE INGREDIENT

Alcohol denat., water, propylene glycol, PEG-40/PPG-8 methylaminopropyl/hydroxypropyl dimethicone copolymer, glycerin, dipropylene glycol, menthol, disodium EDTA, aloe barbadensis leaf juice, isopropyl alcohol, melaleuca alternifolia (tea tree) leaf oil, tocopheryl acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS SCALP ITCH RELIEF 
hydrocortisone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-1414
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MENTHOL (UNII: L7T10EIP3A)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
WATER (UNII: 059QF0KO0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALCOHOL (UNII: 3K9958V90M)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-1414-02	1 in 1 CARTON	08/29/2025
1		68 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/29/2025

Labeler - Walgreens (008965063)

Registrant - Derma Care Research Labs (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(0363-1414)