SHAILEE PSORIASIS TREATMENT- salicylic acid liquid

Shailee Psoriasis Treatment by

Drug Labeling and Warnings

Shailee Psoriasis Treatment by is a Otc medication manufactured, distributed, or labeled by Foshan Sugar Max Cosmetics CO.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient                                            Purpose

Salicylic Acid 3%                                        Psoriasis and Dandruff Seborrheic Dermatitis

PURPOSE

Uses

Controls flaking, scaling, and itching associated with dandruff.

Warnings

For external use only

Do not use

• On a damaged or inflamed scalp.
• If you are allergic to ingredients in this product.

When using this product

• Avoid contact with the eyes.
• If contact occurs, rinse the eyes thoroughly with water.

Stop use and ask a doctor if

• Rash appears.
• condition worsens or does not improve in 2-4 weeks.

If pregnant or breast-feeding, ask a doctor before use.

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

KEEP OUT OF REACH OF CHILDREN

Directions

• Adults and children aged 12 and over.:
  • Wet hair thoroughly.
  • Apply shampoo, generously lather, then rinse thoroughly.
  • Repeat. Use every 3-4 days for up to 8 weeks or as directed by a doctor. Then use only as needed to control dandruff.
• Children under 12 years old.:
  • Ask a doctor.

Other information

• store between 20° – 25°C (68° – 77°F)
• See bottom panel for lot number and expiration date

Inactive ingredients

Purified Water, Sodium C-4-16 Olefin Sulfonate, Cocamidopropyl Betaine, PEG-120 Methyl Glucose Dioleate, Polyquaternium-7, Trolamine, Phospholipid EFA, DL Panthenol USP Powder, Vitamin E Acetate, Biotin, Hydrolyzed Keratin, Oxidized Keratin, Rosemary Oil, Tea Tree Oil, Peppermint Oil,Green Tea Extract, Ascorbic Acid, Manuka Honey

Product label

INGREDIENTS AND APPEARANCE

SHAILEE PSORIASIS TREATMENT 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84938-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
TROLAMINE (UNII: 9O3K93S3TK)
PANTHENOL (UNII: WV9CM0O67Z)
TEA TREE OIL (UNII: VIF565UC2G)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BIOTIN (UNII: 6SO6U10H04)
HYDROLYZED SHEEP WOOL KERATIN (200 MW) (UNII: R6K7AW17SU)
ROSEMARY OIL (UNII: 8LGU7VM393)
PEPPERMINT OIL (UNII: AV092KU4JH)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ASCORBIC ACID (UNII: PQ6CK8PD0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84938-008-01	1 in 1 CARTON	10/30/2025
1		200 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	10/30/2025

Labeler - Foshan Sugar Max Cosmetics CO.,Ltd (700689935)