NEOKETRAMIN ANTIFUNGAL DANDRUFF SEBORRHEIC DERMATITIS PSORIASIS TREATMENT- salicylic acid liquid

Neoketramin Antifungal Dandruff Seborrheic Dermatitis Psoriasis Treatment by

Drug Labeling and Warnings

Neoketramin Antifungal Dandruff Seborrheic Dermatitis Psoriasis Treatment by is a Otc medication manufactured, distributed, or labeled by Rida LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid 3%

Purpose

Psoriasis Dandruff
Seborrheic Dermatitis

Uses

Relieves and helps prevent recurrence of scalp:

• irritation
• itching
• redness
• flaking
• scaling due to psoriasis and seborrheic dermatitis

KEEP OUT OF REACH OF CHILDREN

Directions

• Adults and children aged 12 and over:
  • wet hair thoroughly
  • Apply shampoo, generously lather, then rinse thoroughly. Repeate
  • 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.

Warnings

For external use only
Do not use

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

When using this product

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

Stop use and ask a doctor if:

• Rash appears
• Condition worsen 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.

Inactive ingredients

Ascorbic Acid, Cocamidopropyl Betaine, DL Panthenol USP Powder, Green Tea Extract, Linolemidopropyl PG-Dimonium Chloride Phosphate, PEG-120 Methyl Glucose Dioleate, Polyquaternium-7, Propylene Glycol, Puried Water, Sodium C-14-16 Olefin Sulfonate, Tea Tree Oil, Trolamine, Vitamin E Acetate

Product label

INGREDIENTS AND APPEARANCE

NEOKETRAMIN ANTIFUNGAL DANDRUFF SEBORRHEIC DERMATITIS PSORIASIS TREATMENT 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83004-019
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TEA TREE OIL (UNII: VIF565UC2G)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ASCORBIC ACID (UNII: PQ6CK8PD0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83004-019-01	1 in 1 CARTON	02/28/2025
1		200 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	02/28/2025

Labeler - Rida LLC (004425803)