ACCALLO FUNGAL NAIL PATCHES- fungal nail patches patch

Accallo Fungal Nail Patches by

Drug Labeling and Warnings

Accallo Fungal Nail Patches by is a Otc medication manufactured, distributed, or labeled by Shenzhen Situya Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Tolnaftate 1%

Purpose

Anti-Fungal

Use

Repairs fungal nail damage and improves nail appearance

Warnings

For external use only.

Do not use

■ Do not use if you are allergic to any of the ingredients

■ Do not use if you are pregnant or breastfeeding

When Using

■ Avoid direct contact with eyes, mouth, mucous membrane, wounds

Stop Use

■ if irritation occurs and discomfort persists

Ask Doctor

■ if you have diabetes or poor blood circulation

Keep Oot Of Reach Of Children

■ In case of contact with eyes, flush with water for at least 15 minutes.
■ If swallowed, seek medical assistance immediately or contact a Poison Control Center.

Directions

■ Clean and thoroughly dry the affected area before application.

■ Peel off the patch's protective film, starting with the outer side and then the inner side.

■ Place the sticky side of the patch directly onto the infected area on the nail and remove the release paper.

■ Gently wrap the sides of the toe or finger to ensure a snug fit.

■ Fold the remaining adhesive part to cover the toe/fingertip.

■ Leave the patch on for 6–8 hours (It is recommended to use overnight for 3–6 months).

Other information

■ Store at room temperature and keep away from direct sunlight.
■ Skin discoloration may occur during or after use.

Inactive ingredients

Polyester Spandex, Acrylate Copolymer, Tackifying Resin, Glycerin, Water, Silicone Oil Paper

Questions

Accallo LLC
1405 DEWAR DR. #1324
ROCK SPRINGS, WY 82901
Phone: 1-307-522-6324
Email: info@accallo.com
Website: www.accallo.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACCALLO FUNGAL NAIL PATCHES 
fungal nail patches patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82739-018
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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
ACRYLIC ACID (UNII: J94PBK7X8S)
DICLORAN (UNII: F0BE9UC5J7)
POLYESTER-7 (UNII: 0841698D2F)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82739-018-01	32 in 1 BOX; Type 0: Not a Combination Product	04/07/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	04/07/2024

Labeler - Shenzhen Situya Trading Co., Ltd. (706154255)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Situya Trading Co., Ltd.		706154255	manufacture(82739-018) , label(82739-018)