SINTONG

Manufacturer
Handock Cosmetics Co., Ltd.
Effective date
2017-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:16:28

Label at a glance#

ProductSINTONG
Active ingredientMENTHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 6.0%

INACTIVE INGREDIENT SECTION

Water, Alcohol, PEG-60 Hydrogenated castor oil, Propylene glycol , Butylene glycol, Aspergillus/Rice ferment filtrate, Hamamelis virginiana (Witch hazel) extract, Portulaca oleracea extract, Aloe barbadensis leaf extract, Allantoin, Chlorphenesin, Carbomer, Nonoxynol -12, Triethanolamine, Fragrance

OTC - PURPOSE SECTION

Topical Analgesic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Features : This is a sports massage cream which helps to relieve pain on muscles and joints after a workout. It gives you fresh usability without being sticky.

Usage : The cream is an anti-inflammatory pain relieving and topical analgestic ointment that is intended to relieve muscle and joint pain associated with arthritis, backaches, knee pain and shoulder pain.

WARNINGS SECTION

1) Consult with physician if you develop red, swollen or itchy skin or other abnormal or side effects during or after use owing to direct sunlight.

2) Limit the use on the open wounds.

3) Do not apply this product on the burned skin.

4) For external use only.

5) Avoid contact use eyes.

DOSAGE & ADMINISTRATION SECTION

Apply a suitable amount of cream to the desired area and massage to get it absorbed into the skin.

OTHER SAFETY INFORMATION

Manufacturing No. and Expiry Date : Separately marked

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76369-900176369-9001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b41a96ef-a3f9-4cbe-be81-62109572af9c4f23af51-8428-3d7d-e054-00144ff88e882021-05-12WarningsExact identifier
spl set id: 4f23af51-8428-3d7d-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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