NIZORAL SCALP ITCH RELIEF- hydrocortisone shampoo 
Kramer Laboratories

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Drug Facts

Active ingredientPurpose
Hydrocortisone 1.0%Anti-itch liquid

Uses

Warnings
For external use only. Use only as directed

Flammable. Keep away from fire, or flame.

Do not use

When using this product

Stop use and ask a doctor if

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Other information

Inactive ingredients

alcohol denat., aloe barbadensis leaf juice, dipropylene glycol, disodium EDTA, glycerin, hyaluronic acid, menthol, PEG-12 dimethicone, phenoxyethanol and ethylhexylglycerin, polysorbate-80, tocopheryl acetate, water (aqua)

Questions? 1-800-824-4894

PRINCIPAL DISPLAY PANEL

Nizoral®

Scalp Itch Relief

HYDROCORTISONE 1%
ANTI-ITCH LIQUID 


RELIEVES SCALP ITCH
from seborrheic dermatitis,
psoriasis & eczema

SOOTHES, CALMS & HYDRATES
plus aloe, menthol & hyaluronic acid

MAXIMUM STRENGTH
anti-itch medicine

fragrance-free • greaseless formula

2 fl oz (60mL)

NIZORAL®
Scalp Itch Relief

contains maximum strength
medicine (Hydrocortisone
1%) to relieve scalp itch.
The special medicated
solution helps soothe, calm,
& hydrate an itchy, irritated
scalp; plus it contains
aloe, menthol, vitamin E
& hyaluronic acid. The
tapered bottle tip design
helps easily apply the
medicated solution that's
paraben free, fragrance
free, and greaseless.

Specially 
formulated with:

√ Aloe
√ Menthol
√ Hyaluronic Acid
√ Vitamin E

Before use, read all label information.
If you have a drug reaction, contact a
doctor and report it by calling:
1.800.824.4894

KRAMER
LABORITORIES

Distributed by:
Kramer Laboratories, Inc.
Bridgewater, NJ 08807 USA

© 2023 KRAMER LABORATORIES, INC.

Nizoral Scalp Itch Relief Carton
NIZORAL SCALP ITCH RELIEF 
hydrocortisone shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55505-222
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Hydrocortisone (UNII: WI4X0X7BPJ) (Hydrocortisone - UNII:WI4X0X7BPJ) Hydrocortisone10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Alcohol (UNII: 3K9958V90M)  
Aloe (UNII: V5VD430YW9)  
Dipropylene Glycol (UNII: E107L85C40)  
Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)  
Glycerin (UNII: PDC6A3C0OX)  
Hyaluronic Acid (UNII: S270N0TRQY)  
Menthol, Unspecified Form (UNII: L7T10EIP3A)  
Peg-12 Dimethicone (300 Cst) (UNII: ZEL54N6W95)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Polysorbate 80 (UNII: 6OZP39ZG8H)  
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55505-222-291 in 1 CARTON01/01/2024
160 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/01/2024
Labeler - Kramer Laboratories (122720675)

Revised: 1/2024
Document Id: 492cc472-0e56-4e55-8ff4-e11a963f0aad
Set id: dba59238-6beb-447e-8c4c-e4bc00fd2c20
Version: 2
Effective Time: 20240105
 
Kramer Laboratories