DRYELLO TOLNAFTATE 1% ANTIFUNGAL- tolnaftate stick

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

• Cures most Athlete's Foot (tinea pedis)
• Relieves itching, burning, cracking, and scaling
• Prevents recurrence of most Athlete's foot with daily use

Warnings

Do not use on children under 2 years of age unless directed by a doctor.

For external use only. Avoid contact with eyes.

When using this product

• If irritation occurs, discontinue use and consult a doctor

Keep out of reach of children

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

Directions

• Wash feet and dry thoroughly.
• Apply a think layer of the product to the affected area twice daily (morning and night).
• Supervise children in the use of this product.
• Pay special attention to spaces between toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.

Other

Store between 68º - 86ºF (20º - 30ºC)

Inactive ingredients

Aluminum Hydroxide, Arrowroot Powder, Behenyl Behenate, C12-15 Alkyl Benzoate, Cyclopentasiloxane, Magnesium Aluminum Silicate, Magnesium Citrate, Magnesium Hydroxide, Magnesium Sulfate, Orange Peel Oil, Stearyl Alcohol, Tocopheryl Acetate.

Questions?

1-800-452-7362 dryello.com

Principal Display Panel

For Athlete's Foot

Treats + Prevents

New Silky Smooth Application

Dryello TM

TOLNAFTATE 1% ANTIFUNGAL

Vlinically Proven
Dermatologist Developed

Two Glide-On Sticks

Two 15g (0.53oz) NET WT Sticks

INGREDIENTS AND APPEARANCE

DRYELLO TOLNAFTATE 1% ANTIFUNGAL 
tolnaftate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85565-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
MARANTA ARUNDINACEA ROOT (UNII: FVN346W31A)
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
MAGNESIUM CITRATE (UNII: RHO26O1T9V)
BEHENYL BEHENATE (UNII: K8NU647RJ0)
ORANGE OIL (UNII: AKN3KSD11B)
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
MAGNESIUM SULFATE (UNII: DE08037SAB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85565-005-01	2 in 1 BOX	04/03/2026
1		15 g in 1 APPLICATOR; 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	04/03/2026

Labeler - ProPedix, Inc. (119483645)

Establishment
Name	Address	ID/FEI	Business Operations
Columbia Cosmetics Manufacturing, Inc.		068267863	manufacture(85565-005)