ATONO2 OXYGEN BUBBLE FOAM- glycerin liquid

ATONO2 Oxygen Bubble Foam by

Drug Labeling and Warnings

ATONO2 Oxygen Bubble Foam by is a Otc medication manufactured, distributed, or labeled by LAORGANIC Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Glycerin

INACTIVE INGREDIENT

Disodium Cocoyl Glutamate, Decyl Glucoside, Potassium Cocoyl Glycinate, Disodium Cocoamphodiacetate, Betaine, Potassium Cocoate, Panthenol, etc.

PURPOSE

Skin Protectant

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Pump an appropriate amount and gently massage the wet facial skin with it. Then rinse with warm water.

WARNINGS

• For external use only
• When using this product

1. If any one of following symptoms occurs when using cosmetics, stop using it and consult a dermatologist.
A. red spot, swelling, itching, stimulus
B. symptoms mentioned above are caused by sunlight.

2. Do not apply on skin where there is wound, eczema, or irritation.

3. Storage and cautions for handling
A. Close stopper after using.
B. Keep out of reach of children.
C. Keep away from high or low temperature and direct sunlight.

4. This is not a medicinal product. Made of 100% cosmetic ingredients, it is a sensitive-skin care product for all skin types.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ATONO2 OXYGEN BUBBLE FOAM 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70993-0004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	3.075 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BETAINE (UNII: 3SCV180C9W)
WATER (UNII: 059QF0KO0R)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70993-0004-1	150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/01/2014

Labeler - LAORGANIC Co., Ltd. (689844148)

Registrant - LAORGANIC Co., Ltd. (689844148)

Establishment
Name	Address	ID/FEI	Business Operations
LAORGANIC Co., Ltd.		689844148	manufacture(70993-0004)