DR. B ANTI POLLUTION BUBBLE MASK- glycerin liquid

Dr. B Anti Pollution Bubble Mask by

Drug Labeling and Warnings

Dr. B Anti Pollution Bubble Mask by is a Otc medication manufactured, distributed, or labeled by Ddoruroo Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

glycerin

INACTIVE INGREDIENT

water, sodium chloride, carbonated water, etc

PURPOSE

SKIN PROTECTANT

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

① Put the sheet on the face in a comfortable posture without cleansing
② After 5 to 10 minutes, bubbles begin to remove skin wastes, sebum and fine dust
③ Wait 5 to 10 more minutes, remove the sheet then wash it with lukewarm water or take a shower
④ Finish with appropriate toner

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

DR. B ANTI POLLUTION BUBBLE MASK 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71484-0006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	4 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71484-0006-1	210 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/19/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	12/19/2017

Labeler - Ddoruroo Co., Ltd. (694209410)

Registrant - Ddoruroo Co., Ltd. (694209410)

Establishment
Name	Address	ID/FEI	Business Operations
Ddoruroo Co., Ltd.		694209410	manufacture(71484-0006) , pack(71484-0006) , label(71484-0006)