Nail Treatment Liquid

Manufacturer
Shenzhen Shenyuanye Trading Co., LTD | Guangzhou Mizi Biotechnology Co., Ltd.
Effective date
2024-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:13:33

Label at a glance#

ProductNail Treatment Liquid
Active ingredientCHLORHEXIDINE ACETATE, SALICYLIC ACID
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

SALICYLIC ACID 2%

Chlorhexidine di(acetate) 2%

OTC - PURPOSE SECTION

REMOVES FUNGUS

INDICATIONS & USAGE SECTION

Uses For all caused by nail fungus

nail discoloration

nail thickening

nail splitting

nail crumbling

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

Don't drink, avoid contact with your eye.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Children use it under thesupervision of adults.

OTC - ASK DOCTOR SECTION

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 SECTION

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 SECTION

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

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CHLORHEXIDINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84336-002-012025-07-31C16284748780-13b156c62-2d4b-fb37-e063-e6dba90a4e07Nail Treatment Liquid
84336-002-012025-07-29C16284748780-13b156c62-2d4b-fb37-e063-e6dba90a4e07Nail Treatment Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84336-002-01Nail Treatment Liquid30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84336-002NAIL TREATMENT LIQUID (SALICYLIC ACID, CHLORHEXIDINE DI(ACETATE)) LIQUID [SHENZHEN SHENYUANYE TRADING CO., LTD]11 package rows20240614_18a12de7-2c48-0320-e063-6394a90a3cbc.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84336-00284336-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
18a12de7-2c49-0320-e063-6394a90a3cbc18a12de7-2c48-0320-e063-6394a90a3cbc2024-06-11WarningsExact identifier
spl id: 18a12de7-2c49-0320-e063-6394a90a3cbc
spl set id: 18a12de7-2c48-0320-e063-6394a90a3cbc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.