TOTAL RELIEF- hydrocortisone shampoo

TOTAL RELIEF by

Drug Labeling and Warnings

TOTAL RELIEF by is a Otc medication manufactured, distributed, or labeled by DR. MARDER SKINCARE, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Hydrocortisone 1%

Purpose

Anti-itch liquid

Uses:

helps control the symptoms of scalp itch associated with minor skin irritations and rashes due to

• Seborrheic Dermatitis
• Eczema
• Psoriasis

Warnings:

For external use only.

When using this product

avoid contact with eyes

Stop use and ask a doctor

if condition worsens, symptoms persist for more than 7 days or clear up and occur again.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

• Adults and children 2 years of age and older: Wet hair thoroughly. Apply shampoo, generously lather scalp for several minutes. Rinse thoroughly, Repeat.
• Follow with Step 2 Total Relief Conditioner
• Use daily if needed.

Other Information

• store at room temp. 20° - 25° C (68° - 77° F)

Inactive ingredients

Aqua (Deionized Water), Ascorbic Acid (Vitamin C), Biotin, Caffeine, Camellia Sinensis (Green Tea) Leaf Extract, Caprylyl Glycol, Cocamidopropyl Betaine, Cocos Nucifera (Coconut) Oil, Decyl Glucoside, dl-Panthenol, Glycerin, Glycol Stearate, Hexylene Glycol, Lauryl Glucoside, Lecithin, Methylisothiazolinone, Parfum (Fragrance), Phenoxyethanol, Potassium Sorbate, Propylene Glycol, Resveratrol, Retinyl Palmitate (Vitamin A), Sodium C14-C16 Olefin Sulfonate, Sodium Metabisulfite, Tocopheryl Acetate (Vitamin E), Xanthan Gum

Package Labeling:

INGREDIENTS AND APPEARANCE

TOTAL RELIEF 
hydrocortisone shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71516-342
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
WATER (UNII: 059QF0KO0R)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
BIOTIN (UNII: 6SO6U10H04)
CAFFEINE (UNII: 3G6A5W338E)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCONUT OIL (UNII: Q9L0O73W7L)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCOL STEARATE (UNII: 0324G66D0E)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
RESVERATROL (UNII: Q369O8926L)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71516-342-00	180 mL in 1 TUBE; Type 0: Not a Combination Product	07/25/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/25/2022

Labeler - DR. MARDER SKINCARE, LLC (146890103)