VERACITI- salicylic acid gel

Veraciti by

Drug Labeling and Warnings

Veraciti by is a Otc medication manufactured, distributed, or labeled by The Podiatree Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 17% w/w

Purpose

Wart Remover

Uses

• For the removal of common and plantar warts. The common wart is easily recognized by the rough “cauliflower-like” appearance on the surface.
• The plantar wart is recognized by its location only on the bottom of the foot, its tenderness and the interruption of the footprint pattern.

Warnings

For external use only.

Do not use

on irritated, infected or reddened skin, moles, birthmarks, warts with hair growing from them, warts on the face, genitals or mucous membranes.

Ask a doctor before use if

you are diabetic or have poor circulation.

When using this product

avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes. Avoid inhaling vapors.

Stop use and ask a doctor if

discomfort persists.

Extremely flammable.

Keep away from fire and flame. Cap tube tightly and store at room temperature away from heat.

Keep out of reach of children.

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

Directions

Wash affected area. May soak wart in warm, not hot, water for 5 minutes. Dry affected area thoroughly. Apply one drop at a time to suffciently cover each wart. Let completely dry. Repeat procedure once or twice daily as needed (until wart is removed) for up to 12 weeks.

Inactive ingredients

Flexible Collodion, Glycolic Acid, Hydroxypropylcellulose, Isopropyl Alcohol, Malic Acid, SD 40 Alcohol (43.5%)

Questions or Suggestions?

1.855.763.8733 or visit us at www.thepodiatreecompany.com. Our commitment to you is 100% satisfaction. If you are not

completely satisfied, please contact us directly for a full refund.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VERACITI 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54633-115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	17 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PYROXYLIN (UNII: KYR8BR2X6O)
GLYCOLIC ACID (UNII: 0WT12SX38S)
MALIC ACID (UNII: 817L1N4CKP)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54633-115-15	15 g in 1 TUBE; Type 0: Not a Combination Product	10/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	10/01/2015

Labeler - The Podiatree Company (078656000)