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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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 not finalpart34810/15/2012
Labeler - RB Health (US) LLC (081049410)

Revised: 1/2023
Document Id: f214b48d-aaad-415e-e053-2995a90a06c4
Set id: 7b1a29fa-b266-43e6-a87b-aa3c96ab4041
Version: 6
Effective Time: 20230112
 
RB Health (US) LLC