MedPath

Nail Renewal Liquid

Approved
Approval ID

3d641f1d-ce60-b811-e063-6294a90ad567

Product Type

HUMAN OTC DRUG LABEL

Effective Date

Aug 27, 2025

Manufacturers
FDA

TT Beauty Trading Co., Ltd.

DUNS: 661400516

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

GLYCERIN

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code85206-004
Application NumberM016
Product Classification
M
Marketing Category
C200263
G
Generic Name
GLYCERIN
Product Specifications
Route of AdministrationTOPICAL
Effective DateAugust 27, 2025
FDA Product Classification

INGREDIENTS (5)

AQUAInactive
Quantity: 28.2 mg in 30 mg
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Quantity: 1.2 mg in 30 mg
Code: PDC6A3C0OX
Classification: IACT
ACETIC ACIDInactive
Quantity: 0.15 mg in 30 mg
Code: Q40Q9N063P
Classification: IACT
EDETATE DISODIUMInactive
Quantity: 0.03 mg in 30 mg
Code: 7FLD91C86K
Classification: IACT
SOPHORA FLAVESCENS ROOTActive
Quantity: 0.42 mg in 30 mg
Code: IYR6K8KQ5K
Classification: ACTIB

Drug Labeling Information

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LOINC: 51945-4Updated: 8/28/2025

1

INDICATIONS & USAGE SECTION

LOINC: 34067-9Updated: 8/28/2025

One drop in the morning and one drop in the evening. Use it continuously until it heals.

OTC - ACTIVE INGREDIENT SECTION

LOINC: 55106-9Updated: 8/28/2025

SOPHORA ANGUSTIFOLIA ROOT

STORAGE AND HANDLING SECTION

LOINC: 44425-7Updated: 8/28/2025

Store in a cool and dry place.

OTC - WHEN USING SECTION

LOINC: 50567-7Updated: 8/28/2025

1.For the first use, soak the sick nail in warm water.
2.Thin the irregular nail with a file.
3.Drop an appropriate amount of this product and slowly penetrate into the diseased nail.
4.One drop in the morning and one drop in the evening. Use it continuously until it heals.

OTC - PURPOSE SECTION

LOINC: 55105-1Updated: 8/28/2025

Deep Bacteriostatic
Nourishing Brightening Nail
Remove Bad Nails

OTC - DO NOT USE SECTION

LOINC: 50570-1Updated: 8/28/2025

Discontinue use if signs of irritation or rash occur.

OTC - STOP USE SECTION

LOINC: 50566-9Updated: 8/28/2025

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

LOINC: 50565-1Updated: 8/28/2025

Please keep out of reach of children. Do not swallow.

INACTIVE INGREDIENT SECTION

LOINC: 51727-6Updated: 8/28/2025

AQUA、 GLYCERIN、 ACETIC ACID、DISODIUM EDTA

WARNINGS SECTION

LOINC: 34071-1Updated: 8/28/2025

Please keep out of reach of children. Do not swallow. Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.

DOSAGE & ADMINISTRATION SECTION

LOINC: 34068-7Updated: 8/28/2025

One drop in the morning and one drop in the evening. Use it continuously until it heals.

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Nail Renewal Liquid - FDA Drug Approval Details