Label: VERACITI- salicylic acid gel
- NDC Code(s): 54633-115-15
- Packager: The Podiatree Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated December 20, 2017
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- Active ingredient
Salicylic acid 17% w/wClose
- 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.
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.
When using this product
avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes. Avoid inhaling vapors.
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.
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.Close
- Inactive ingredients
Flexible Collodion, Glycolic Acid, Hydroxypropylcellulose, Isopropyl Alcohol, Malic Acid, SD 40 Alcohol (43.5%)Close
- 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.Close
- PRINCIPAL DISPLAY PANEL
- INGREDIENTS AND APPEARANCE
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) HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P) MALIC ACID (UNII: 817L1N4CKP) 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)