Otc - Active Ingredient
Salicylic Acid 17%
Goodnites Wart Removal Gel Liquid
FDA Label NDC 85578-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhengzhou Hangrui Network Technology Co., Ltd. for the product Goodnites Wart Removal Gel (NDC 85578-005). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Wart remover
Indications & Usage
.For removing common warts and plantar warts
Warnings
For external use only
Otc - Do Not Use
on irritated, infected, or reddened skin
on genital warts or warts on the face
if you have diabetes or poor blood circulation
Otc - When Using
do not use near eyes or mucous membranes
some mild irritation may occur
if excessive irritation occurs, stop use and consult a doctor
Otc - Stop Use
condition worsens
excessive irritation develops
you experience unexpected side effects
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Dosage & Administration
Clean affected area
Apply a thin layer to skin tag using applicator.
Allow to dry fully
Repeat application twice daily for up to 4 weeks or as directed by a doctor
Inactive Ingredient
ALCOHOL
CAMPHOR (NATURAL)
CASTOR OIL
ETHYL ACETATE
HYDROXYPROPYL CELLULOSE (TYPE H)
HYPOPHOSPHOROUS ACID
ISOPROPYL ALCOHOL
PYROXYLIN
POLYSORBATE 80
Package Label.Principal Display Panel
Label2 (Label2)
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