NAIL TREATMENT LIQUID (salicylic acid, chlorhexidine di- acetate liquid

Nail Treatment Liquid by

Drug Labeling and Warnings

Nail Treatment Liquid by is a Otc medication manufactured, distributed, or labeled by Shenzhen Shenyuanye Trading Co., LTD, Guangzhou Mizi Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

SALICYLIC ACID 2%

Chlorhexidine di(acetate) 2%

PURPOSE

REMOVES FUNGUS

INDICATIONS & USAGE

Uses For all caused by nail fungus

nail discoloration

nail thickening

nail splitting

nail crumbling

WARNINGS

For external use on nailfungus(onychomycosis) only, pleasedon't use it on healthy nails.

DO NOT USE

Don't use it on damafed skin,otherwise, your damaged skin maybe painful.

WHEN USING

Don't drink, avoid contact with your eye.

STOP USE

For people with severe skin ulceration, please use it with caution.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

Children use it under thesupervision of adults.

ASK DOCTOR

Stop use and ask a doctor if

You are allergic to vinegar(such as itching, rash sweling ofthe lips, eyelids, and shortnessof breath)

DOSAGE & ADMINISTRATION

Direction
Apply it in the day and night(twice a day).
Before using it for the first time,soak the diseased nail with warm water to soften it, use thenail file to polish the nail, make itthin cisibly, and scrape off thedirt on the nail (be careful not tohurt the nail hed), then apply theliquid.
After first use, every 2-3 daysuse the nail file to polish thesur face of the diseased nail and then continue to use it.
If seallowed, get medical help or contact a poison controlcenter right away.

INACTIVE INGREDIENT

Water, Sorbitol, Alcohol, Propylene-Glycol, Angelica Dahurica,Laurocapram, Caramel, Dimethylol.Urea, Sunset Yellow.

QUESTIONS

For the quesiton, please contact us bybaizelu@outlook.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NAIL TREATMENT LIQUID 
salicylic acid, chlorhexidine di(acetate) liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84336-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE	2 mg  in 100 mL
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
LAUROCAPRAM (UNII: 1F3X9DRV9X)
CARAMEL (UNII: T9D99G2B1R)
WATER (UNII: 059QF0KO0R)
OXYMETHUREA (UNII: N68H97CAWG)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84336-002-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/11/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	06/11/2024

Labeler - Shenzhen Shenyuanye Trading Co., LTD (550376513)

Registrant - Shenzhen Shenyuanye Trading Co., LTD (550376513)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Mizi Biotechnology Co., Ltd.		418001649	manufacture(84336-002)