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 November 19, 2019
If you are a consumer or patient please visit this version.
- Active ingredient
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.
- Inactive ingredients
- Questions or Suggestions?
- 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) 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)