ATONO2 Baby Sun Cream

Manufacturer
LAORGANIC Co., Ltd.
Effective date
2016-10-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:47:31

Label at a glance#

ProductATONO2 Baby Sun Cream
Active ingredientTITANIUM DIOXIDE, OCTINOXATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate, Titanium Dioxide

INACTIVE INGREDIENT SECTION

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.

OTC - PURPOSE SECTION

Skin Protectant - Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Apply proper amount to the skin

WARNINGS SECTION

  • 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 SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ll

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70993-0003-12020-01-31C16284748780-19d75b9d0-09a3-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70993-0003-1ATONO2 Baby Sun Cream50 g in 1 TUBECREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70993-0003ATONO2 BABY SUN CREAM (ETHYLHEXYL METHOXYCINNAMATE, TITANIUM DIOXIDE) CREAM [LAORGANIC CO., LTD.]2Legacy NDC, 1 package rows20161013_3eb67c20-a1b6-3014-e054-00144ff8d46c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70993-000370993-0003-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
GLYCERINPDC6A3C0OXIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3eb6d0de-cea9-3db8-e054-00144ff8d46c3eb67c20-a1b6-3014-e054-00144ff8d46c2016-10-12WarningsExact identifier
spl id: 3eb6d0de-cea9-3db8-e054-00144ff8d46c
spl set id: 3eb67c20-a1b6-3014-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.