SCALPICIN ANTI-ITCH MAXIMUM STRENGTH- hydrocortisone liquid 
RB Health (US) LLC

----------

Scalpicin ®

Anti-Itch Maximum Strength

Drug Facts

Active ingredient

Hydrocortisone 1%

Purpose

Anti-itch liquid

Uses

Warnings

For external use only

Avoid contact with the eyes

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, stop use of this product and do not begin use of any other hydrocortisone product unless you have consulted a doctor

Do not use for the treatment of diaper rash. Consult a doctor.

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

Directions

Other information

Inactive ingredients

Alcohol Denat., Aloe Barbadensis Leaf Juice, Dipropylene Glycol, Disodium EDTA, Glycerin, Melaleuca Alternifolia Leaf Oil, Menthol, PEG-40/PPG-8 Methylaminopropyl/Hydroxypropyl Dimethicone Copolymer, Propylene Glycol, t-Butyl Alcohol, Tocopheryl Acetate, Water

Questions?

1-866-252-5327

You may also report side effects to this phone number.

Distributed by: RB Health (US)
Parsippany, NJ 07054-0224

PRINCIPAL DISPLAY PANEL - 44 mL Bottle Carton

SCALPICIN ®

MAXIMUM

STRENGTH

Hydrocortisone 1% Anti-Itch Liquid

SCALP ITCH RELIEF

on the GO

WITH ALOE

1.5 FL OZ (44 mL)

Label

SCALPICIN  ANTI-ITCH MAXIMUM STRENGTH
hydrocortisone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-851
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
TEA TREE OIL (UNII: VIF565UC2G)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-851-151 in 1 CARTON10/15/2012
144 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01710/15/2012
Labeler - RB Health (US) LLC (081049410)

Revised: 12/2024
Document Id: 29a76de4-1587-8cc2-e063-6294a90a1166
Set id: 7b1a29fa-b266-43e6-a87b-aa3c96ab4041
Version: 7
Effective Time: 20241219
 
RB Health (US) LLC