SINTONG by Handock Cosmetics Co., Ltd. SINTONG- menthol cream

SINTONG by

Drug Labeling and Warnings

SINTONG by is a Otc medication manufactured, distributed, or labeled by Handock Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Menthol 6.0%

INACTIVE INGREDIENT

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

PURPOSE

Topical Analgesic

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

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

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SINTONG 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76369-9001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALLANTOIN (UNII: 344S277G0Z)
PURSLANE (UNII: M6S840WXG5)
WITCH HAZEL (UNII: 101I4J0U34)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76369-9001-1	150 mL in 1 TUBE; Type 0: Not a Combination Product	04/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/01/2017

Labeler - Handock Cosmetics Co., Ltd. (688037204)

Registrant - Handock Cosmetics Co., Ltd. (688037204)

Establishment
Name	Address	ID/FEI	Business Operations
Handock Cosmetics Co., Ltd.		688037204	manufacture(76369-9001) , label(76369-9001) , pack(76369-9001)