Label: TREATONIC WART REMOVER- wart remover ointment
- NDC Code(s): 82739-002-01
- Packager: Shenzhen Situya Trading Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated August 8, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
-
When using this product
Do not use .
on irritated skin or on any area that is infected or reddened .
Do not use on moles, skin tags, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranesAsk a doctor before you use
if vou haveliabetes or poor blood circulationStop use and ask a doctor
if discomfort persistsKeep out of reach of children
lf product getsnto eves, flush with water for 15 minutes
lf swallowed. get medical help or contact a Poison Control Center right away - Stop use
- KEEP OUT OF
- Directions
- Other information
- Inactive ingredients
- Questions?
- Package Label-principal Display Panel
-
INGREDIENTS AND APPEARANCE
TREATONIC WART REMOVER
wart remover ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82739-002 Route of Administration EXTRACORPOREAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 17 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PHELLODENDRINE (UNII: AR68S526RB) CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) OSTHOL (UNII: XH1TI1759C) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) XANTHAN GUM (UNII: TTV12P4NEE) ACETIC ACID (UNII: Q40Q9N063P) ANGELICA SINENSIS ROOT (UNII: B66F4574UG) ANGELICA DAHURICA LEAF (UNII: ONF5ZKM88G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82739-002-01 15 mL in 1 BOX; Type 0: Not a Combination Product 12/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/06/2022 Labeler - Shenzhen Situya Trading Co., Ltd. (706154255) Establishment Name Address ID/FEI Business Operations Shenzhen Situya Trading Co., Ltd. 706154255 manufacture(82739-002)