NailSpray

Manufacturer: Shenzhen Hengkaifeng Commerce and Trade Co., Ltd
Effective date: 2024-10-15
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:25:35

Label at a glance#

ProductNailSpray

Active ingredientSALICYLIC ACID, EUCALYPTOL

Label structure10 sections

Indications and uses

Uses for relief and treatment of pain,soreness, and inflammation from nail fungus. Symptoms: ■ discolored nails ■ brittle nails ■ distorted nails

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid

PURPOSE

OTC - PURPOSE SECTION

Anti-fungal

Uses

INDICATIONS & USAGE SECTION

Uses for relief and treatment of pain,soreness, and inflammation from nail fungus.
Symptoms: ■ discolored nails ■ brittle nails ■ distorted nails

Warnings

WARNINGS SECTION

For external use only, Some individuals may be sensitive to essential oils.
Begin with a small drop to determine if product causes any irritation. Discontinue use if any irritation occurs.
Stop use and consult a doctor if condition worsens, Not for use on children under the age of 2 without physician direction.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occur

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skik

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallwed, get medical help or contact a Poison Control Center right away.

inactive ingredients

INACTIVE INGREDIENT SECTION

Water

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

shake well before use.Wash and thoroughly dry the affectedarea. Apply 1-2 drops and gently rubinto affected area three times per day.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84117-030-01	NailSpray	20 mL in 1 BOTTLE	LIQUID	20		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84117-030	NAILSPRAY (NAIL SPRAY) LIQUID [SHENZHEN HENGKAIFENG COMMERCE AND TRADE CO., LTD]	1	1 package rows	20241017_2484d41a-c8df-211d-e063-6394a90abaa1.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NailSpray
Nail Spray
WATER
SALICYLIC ACID
EUCALYPTOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84117-030	84117-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SALICYLIC ACID	O414PZ4LPZ	ACTIB
EUCALYPTOL	RV6J6604TK	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2484d41a-c8e0-211d-e063-6394a90abaa1			2484d41a-c8df-211d-e063-6394a90abaa1	2024-10-15	Warnings	Exact identifier spl id: 2484d41a-c8e0-211d-e063-6394a90abaa1 spl set id: 2484d41a-c8df-211d-e063-6394a90abaa1

Reported adverse events (FAERS/openFDA)#

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