ABELIA CUCUMBER SOOTHING MASK- dipropylene glycol liquid

Abelia cucumber soothing mask by

Drug Labeling and Warnings

Abelia cucumber soothing mask by is a Otc medication manufactured, distributed, or labeled by TERRASUN CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

dipropylene glycol

INACTIVE INGREDIENT

water, betaine, etc.

PURPOSE

skin protectant

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

place mask on face and remove after 15-20 minutes

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ABELIA CUCUMBER SOOTHING MASK 
dipropylene glycol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70202-0005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPROPYLENE GLYCOL (UNII: E107L85C40) (DIPROPYLENE GLYCOL - UNII:E107L85C40)	DIPROPYLENE GLYCOL	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BETAINE (UNII: 3SCV180C9W)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70202-0005-1	24 g in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/28/2016

Labeler - TERRASUN CO., LTD. (689605807)

Registrant - TERRASUN CO., LTD. (689605807)

Establishment
Name	Address	ID/FEI	Business Operations
TERRASUN CO., LTD.		689605807	manufacture(70202-0005)