SOUTH MOON Ingrown Toenail Drops

Manufacturer
Shantou South Moon Biotechnology Co., Ltd.
Effective date
2025-11-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:18:27

Label at a glance#

ProductSOUTH MOON Ingrown Toenail Drops
Active ingredientTHYMUS VULGARIS (THYME) FLOWER/LEAF OIL, COMMIPHORA MYRRHA RESIN
Label structure12 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

COMMIPHORA MYRRHA RESIN、THYMUS VULGARIS (THYME) FLOWER/LEAF OIL

OTC - WHEN USING SECTION

Drop the toenail onto the affected toe,until the nail can get out of the groove Take out and trim easily.

OTC - PURPOSE SECTION

SOFTENS IN-GROWING TOENAIL
IMPROVE TOENAIL HEALTH
EFFECTIVE AND GENTLE

WARNINGS SECTION

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.

OTC - DO NOT USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

STORAGE AND HANDLING SECTION

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

AQUA、GLYCERIN、PANTHENOL、SODIUM PCA

DOSAGE & ADMINISTRATION SECTION

Drop the toenail onto the affected toe,until the nail can get out of the groove Take out and trim easily.

INDICATIONS & USAGE SECTION

Drop the toenail onto the affected toe,until the nail can get out of the groove Take out and trim easily.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84983-014-01SOUTH MOON Ingrown Toenail Drops30 mg in 1 BOTTLELIQUID302

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84983-01484983-014-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
449f0078-532d-6d4f-e063-6294a90af04a3f10b998-49c7-f2b0-e063-6294a90ac7bf2025-11-27WarningsExact identifier
spl id: 449f0078-532d-6d4f-e063-6294a90af04a
spl set id: 3f10b998-49c7-f2b0-e063-6294a90ac7bf

Reported adverse events (FAERS/openFDA)#

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