NDC 81799-004

Wart Remover

Zitalon Wart Removal Treatment Liquid

Wart Remover is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Ehy Holdings Llc. The primary component is Salicylic Acid.

Product ID81799-004_ebda964a-6984-9082-e053-2a95a90a0e5e
NDC81799-004
Product TypeHuman Otc Drug
Proprietary NameWart Remover
Generic NameZitalon Wart Removal Treatment Liquid
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2022-10-25
Marketing CategoryOTC MONOGRAPH FINAL /
Application Numberpart358B
Labeler NameEhy Holdings LLC
Substance NameSALICYLIC ACID
Active Ingredient Strength12 mg/100mL
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 81799-004-01

15 mL in 1 BOTTLE (81799-004-01)
Marketing Start Date2022-10-25
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Wart Remover" or generic name "Zitalon Wart Removal Treatment Liquid"

NDCBrand NameGeneric Name
28691-0400Wart RemoverSalicylic Acid
57955-0818Wart RemoverAntimonium crudum, Causticum, Dulcamara, Kali muriaticum, Nitricum acidum, Sabina, Staphysagria, Sulfur, Thuja occidentalis
81799-004Wart RemoverZITALON Wart Removal Treatment Liquid
11822-0134Salicylic acidWart Remover
36800-377Salicylic acidWart Remover
42507-133Salicylic acidWart Remover
55315-375Salicylic acidWart Remover
68016-611Salicylic AcidWart Remover
82739-002Treatonic Wart RemoverWart Remover

Trademark Results [Wart Remover]

Mark Image

Registration | Serial
Company
Trademark
Application Date
WART REMOVER
WART REMOVER
97797120 not registered Live/Pending
Jiang Yanwen
2023-02-16

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.