Nail Strengthen Cream

Manufacturer: Shenzhen Hengkaifeng Commerce and Trade Co., Ltd
Effective date: 2024-08-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:17:06

Label at a glance#

ProductNail Strengthen Cream

Active ingredientTOLNAFTATE

Label structure11 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

Tolnaftate ≤1%

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 people may be sensitive to essential oils.
to determine if the product may cause any irritation. Discontinue use if any irritation occurs.
If condition worsens, discontinue use and consult a physician. Not suitable for use by children under 2 years of age without a physician's guidance.

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

When using this product

OTC - WHEN USING SECTION

Wash and thoroughly dry the affected area.
Three times a day, rub gently onto the affected area.
Wash hands after applying

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

Propylene Glycol

Hydrogenated Castor Oil

Glycerin

Vena Sativa Peptide

Salvia Miltiorrhiza Leaf Extract

Centella Asiatica Extract

Leonurus Artemisia Powder

Arnica Montana Extract

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Wash and dry affected area thoroughly before use. Apply gently to affected area 3 times daily.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
103951	tolnaftate 1 % Topical Cream	PSN	1
103951	tolnaftate 10 MG/ML Topical Cream	SCD	1
103951	tolnaftate 1 % Topical Cream	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
84117-022-01	2026-01-29	C162847	48780-1	49896155-a5e1-586f-e063-e6dba90add90	1f7c0be2-522d-f694-e063-6294a90ae50a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84117-022-01	Nail Strengthen Cream	20 g in 1 CANISTER	CREAM	20		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84117-022	NAIL STRENGTHEN CREAM CREAM [SHENZHEN HENGKAIFENG COMMERCE AND TRADE CO., LTD]	1	1 package rows	20240814_1f7c0be2-522d-f694-e063-6294a90ae50a.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Nail Strengthen Cream
WATER
TOLNAFTATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84117-022	84117-022-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
TOLNAFTATE	06KB629TKV	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
1f7c0be2-522e-f694-e063-6294a90ae50a			1f7c0be2-522d-f694-e063-6294a90ae50a	2024-08-12	Warnings	Exact identifier spl id: 1f7c0be2-522e-f694-e063-6294a90ae50a spl set id: 1f7c0be2-522d-f694-e063-6294a90ae50a

Reported adverse events (FAERS/openFDA)#

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