Label: SCALPICIN ANTI-ITCH MAXIMUM STRENGTH- hydrocortisone liquid
- NDC Code(s): 63824-851-15
- Packager: RB Health (US) LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 19, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
-
Directions
- adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
- children under 2 years of age: do not use; consult a doctor
- twist the flow-control cap to open
- apply at first signs of itching
- if using after shampooing, towel dry hair
- apply from bottle directly to scalp, massage in
- to avoid running or dripping, do not squeeze bottle too hard
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 44 mL Bottle Carton
-
INGREDIENTS AND APPEARANCE
SCALPICIN ANTI-ITCH MAXIMUM STRENGTH
hydrocortisone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63824-851 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 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:63824-851-15 1 in 1 CARTON 10/15/2012 1 44 mL in 1 BOTTLE, DISPENSING; 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 10/15/2012 Labeler - RB Health (US) LLC (081049410)