FDA.reportPublic FDA data

ATOMY SUN CREAM SPF 50 PA

Manufacturer
ATOMY CO LTD
Effective date
2010-04-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:53:05

Label at a glance#

ProductATOMY SUN CREAM SPF 50 PA
Active ingredientOCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
Label structure2 sections

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Octinoxate 7.5%
Octisalate 5.0%
Zinc Oxide 4.9%
Titanium Dioxide 2.49%

Uses
Helps prevent sunburn. Provides High protect from sunburn. Highter SPF gives more sunburn protection.

Directions
Apply after basic skin care product. Spread and appropriate amount entire face following the skin texture. Reapply as required.

Warnings
For external use only.
UV exposure from the sun increases the risk of skin cancer, premature skin aging, and other skin damage. It is important to decrease UV exposure by limiting time in the sun, wearing protective clothing, and using a sunscreen.
When using the product Keep out of eyes. Rinse with water to remove.
Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ATOMY SUNCREAM SPF 50+PA+++

60ml/2fl.oz

image of carton labelimage of carton label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52257-1001-22020-11-03C16284748780-1956f9ecf-cc2a-621f-e053-dbdaa90a74adATOMY SUNCREAM SPF 50+PA+++
52257-1001-22019-10-21C16284748780-1956f9ecf-cc2a-621f-e053-dbdaa90a74adATOMY SUNCREAM SPF 50+PA+++

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
OCTISALATEACTIVE INGREDIENT4X49Y0596W2
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP2
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z2
OCTINOXATEACTIVE MOIETY4Y5P7MUD512
OCTISALATEACTIVE MOIETY4X49Y0596W2
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP2
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z2

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
52257-100152257-1001-1, 52257-1001-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
70157590-222e-4997-828c-13f6e2016638ccd7afd2-e654-4a2f-a5f8-6214a9d3a3402020-11-02WarningsExact identifier
spl set id: ccd7afd2-e654-4a2f-a5f8-6214a9d3a340

Reported adverse events (FAERS/openFDA)#

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