Label: WALGREENS SCALP RELIEF EXTERNAL ANALGESIC- hydrocortisone liquid
- NDC Code(s): 0363-9068-01
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 18, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
-
Warnings
Flammable. Keep away from fire or flame.
For external use only.
When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water. If Irritation persists, consult a doctor.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 74 mL Bottle Carton
VALUE SIZE
Walgreens
• WALGREENS •
PHARMACIST RECOMMENDEDCompare to the active ingredient in
Maximum Strength Scalpicin®††Scalp
ReliefHYDROCORTISONE 1% /
SEBORRHEIC DERMATITIS /
PSORIASIS ANTI-ITCH LIQUIDMaximum Strength
+ Vitamin E
- Helps stop intense scalp
itch associated with
psoriasis, flaking &
seborrheic dermatitis
2.5 FL OZ (74 mL)
- Helps stop intense scalp
-
INGREDIENTS AND APPEARANCE
WALGREENS SCALP RELIEF EXTERNAL ANALGESIC
hydrocortisone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-9068 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ALOE VERA LEAF (UNII: ZY81Z83H0X) Dipropylene Glycol (UNII: E107L85C40) EDETATE DISODIUM (UNII: 7FLD91C86K) Glycerin (UNII: PDC6A3C0OX) Isopropyl Alcohol (UNII: ND2M416302) TEA TREE OIL (UNII: VIF565UC2G) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) Propylene Glycol (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) Water (UNII: 059QF0KO0R) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-9068-01 1 in 1 CARTON 10/30/2023 1 74 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 10/30/2023 Labeler - Walgreen Company (008965063) Registrant - Garcoa, INC (036464697) Establishment Name Address ID/FEI Business Operations Sigan Industries INC 255106239 MANUFACTURE(0363-9068) , LABEL(0363-9068) , PACK(0363-9068)