GOODNITES SKIN TAG REMOVER- salicylic acid liquid

Goodnites skin tag remover by

Drug Labeling and Warnings

Goodnites skin tag remover by is a Otc medication manufactured, distributed, or labeled by Zhengzhou Hangrui Network Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 17%

PURPOSE

Wart remover

KEEP OUT OF REACH OF CHILDREN

lf swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

For the removal of common warts and plantar warts.

WARNINGS

For external use only.

WHEN USING

avoid contact with eyes and mucous membranes
some mild irritation may occur; if excessive irritation occurs stop use and ask a doctor

STOP USE

condition worsens
excessive irritation develops
you experience unexpected side effects

DO NOT USE

on irritated, infected, or reddened skin
on moles, birthmarks, warts with hair, genital warts, warts on the face, or on mucous membranes
if you have diabetes or poor blood circulation

DOSAGE & ADMINISTRATION

adults and children 2 years and over:
wash affected area (optional: soak wart in warm water for 5 minutes).
dry area thoroughly.
apply one drop/small amount at a time with applicator/brush to sufficiently cover each wart
let dry
repeat once or twice daily as needed (until wart is removed) for up to 12 weeks
children under 2 years: ask a doctor

INACTIVE INGREDIENT

Glycerin, Polyethylene Glycol, Water, Borneol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOODNITES SKIN TAG REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85578-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BORNEOL (UNII: M89NIB437X)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85578-002-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/29/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	05/29/2025

Labeler - Zhengzhou Hangrui Network Technology Co., Ltd. (700094663)

Establishment
Name	Address	ID/FEI	Business Operations
Zhengzhou Hangrui Network Technology Co., Ltd.		700094663	manufacture(85578-002)