ATONO2 BABY SUN CREAM- ethylhexyl methoxycinnamate, titanium dioxide cream

ATONO2 Baby Sun Cream by

Drug Labeling and Warnings

ATONO2 Baby Sun Cream by is a Otc medication manufactured, distributed, or labeled by LAORGANIC Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethylhexyl Methoxycinnamate, Titanium Dioxide

INACTIVE INGREDIENT

Glycerin, Cyclomethicone, Cyclopentasiloxane, Isoamyl p-methoxycinnamate, Cyclohexasiloxane, Butylene Glycol, Cetyl Alcohol, Potassium Cetyl Phosphate, Glyceryl Stearate, Hydrogenated Polyisobutene, Bis-Ethylhexyloxyphenol Methoxyphenyl, Triazine, PEG-10 Dimethicone, Dimethicone, PEG-100 Stearate, etc.

PURPOSE

Skin Protectant - Sunscreen

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Apply proper amount to the skin

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 BABY SUN CREAM 
ethylhexyl methoxycinnamate, titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70993-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.97 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70993-0003-1	50 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	09/01/2016

Labeler - LAORGANIC Co., Ltd. (689844148)

Registrant - LAORGANIC Co., Ltd. (689844148)

Establishment
Name	Address	ID/FEI	Business Operations
LAORGANIC Co., Ltd.		689844148	manufacture(70993-0003)