TIO NACHO ANTI-DANDRUFF- salicylic acid liquid

Tio Nacho Anti-Dandruff by

Drug Labeling and Warnings

Tio Nacho Anti-Dandruff by is a Otc medication manufactured, distributed, or labeled by Genomma Lab USA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient

Salicylic Acid 2.2%

Purpose

Anti-Dandruff

Use

For relief of the symptoms of dandruff.

• Helps prevent recurrence of flaking, itching or irritation.
• Helps control the itching associated with dandruff.

Warnings

For external use only.

When using this product Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Consult a doctor if condition worsens or does not improve after regular use of this product as directed.

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

Directions

For best results use at least twice a week or as directed by a doctor.

• Wet hair thoroughly
• Apply the shampoo into the scalp and massage
• Lather and leave on hair and scalp for several minutes
• Rinse and repeat.

Other Information

Store at room temperature.

• Keep product away from direct sunlight.

Inactive Ingredients

Water, sodium laureth sulfate, cocamide MIPA, cocamidopropyl betaine, fragrance, sodium hydroxide, glycol distearate, propylene glycol, royal jelly extract, laureth-4, polyquaternium-10, disodium EDTA, polyquaternium-7, benzotriazolyl dodecyl p-cresol, honey extract, methylchloroisothiazolinone, methylisothiazolinone.

Questions?

Call toll free 1-877-994-3666

Monday to Friday, 8am to 6pm, Central time

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Distributed by:
Genomma Lab USA Inc.,
Houston, TX, 77098

PRINCIPAL DISPLAY PANEL - 415 ml Bottle Carton

TÍO
NACHO®

SHAMPOO

ANTI-HAIR LOSS*
*DUE TO BREAKAGE

ANTI-DANDRUFF
SHAMPOO
SALICYLIC ACID 2.2%

ROYAL JELLY

FOR RELIEF OF THE SYMPTOMS
OF DANDRUFF

100%
RECYCLED°
& RECYCLABLE
PACKAGING

14 FL OZ. (415 ml)

INGREDIENTS AND APPEARANCE

TIO NACHO ANTI-DANDRUFF 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50066-059
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic acid (UNII: O414PZ4LPZ) (Salicylic acid - UNII:O414PZ4LPZ)	Salicylic acid	22 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
cocamidopropyl betaine (UNII: 5OCF3O11KX)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
laureth-4 (UNII: 6HQ855798J)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Product Characteristics
Color	BROWN (brown)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50066-059-14	1 in 1 CARTON	03/27/2026
1		415 mL in 1 BOTTLE, PLASTIC; 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	03/27/2026

Labeler - Genomma Lab USA (832323534)