SHYNOMORE LUBRICANT- centella asiatica extract gel

SHYNOMORE LUBRICANT by

Drug Labeling and Warnings

SHYNOMORE LUBRICANT by is a Otc medication manufactured, distributed, or labeled by Bluette Co., Ltd., Daeduck Lab. Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Centella Asiatica Extract

INACTIVE INGREDIENT

Sodium Hyaluronate, Hamamelis Virginiana (Witch Hazel) Leaf Extract, etc.

PURPOSE

Water-soluble massage gel

KEEP OUT OF REACH OF CHILDREN

keep out or reach of the children

INDICATIONS & USAGE

With clean hands, dispense an appropriate amount and apply on skin, massaging gently

WARNINGS

Precautions for Use

If any of the following conditions occur, discontinue use immediately and consult a dermatologist. Continuous use will cause symptoms to worsen.

1) In case of skin reaction such as red spots, swelling, itch or irritation etc. during use

2) In case of the above skin reaction when applied area is exposed to direct sunlight

Do not use on damaged skin area such as wound, rash or skin infection

Storage and Handling

1) Close lid tightly after use

2) Keep out of reach of infants and children

3) Store in a cool, dry place away from direct sunlight

4) Avoid eye area

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SHYNOMORE LUBRICANT 
centella asiatica extract gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72072-0001
Route of Administration	VAGINAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CENTELLA ASIATICA (UNII: 7M867G6T1U) (CENTELLA ASIATICA - UNII:7M867G6T1U)	CENTELLA ASIATICA	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72072-0001-1	100 mL in 1 TUBE; Type 0: Not a Combination Product	01/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/01/2018

Labeler - Bluette Co., Ltd. (694855403)

Registrant - Bluette Co., Ltd. (694855403)

Establishment
Name	Address	ID/FEI	Business Operations
Daeduck Lab. Co.,Ltd.		557819376	manufacture(72072-0001)

Establishment
Name	Address	ID/FEI	Business Operations
Bluette Co., Ltd.		694855403	label(72072-0001)