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United States · US · US:52257-1400_d9c210b4-3004-44e0-a417-0394f5af6302
ATOMY DERMA CALMING SUN
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerATOMY CO., LTD.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11522571400116 g in 1 CARTON (52257-1400-1)
Annotations
UNII (FDA Substance ID)
15FIX9V2JP
TITANIUM DIOXIDE
RxCUI 38323
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "15FIX9V2JP",
"rxcui": "38323",
"inchikey": "SOQBVABWOPYFQZ-UHFFFAOYSA-N",
"display_name": "TITANIUM DIOXIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"994d5680-284e-4faf-a29b-4d28f8d46e8f": {
"match": "brand_token",
"title": "ATOMY SUNSCREEN BEIGE BROAD SPECTRUM SPF 50 PLUS (HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE) CREAM [ATOMY CO., LTD.]",
"spl_version": "3",
"published_date": "2024-12-06"
}
},
"productid": "52257-1400_d9c210b4-3004-44e0-a417-0394f5af6302",
"productndc": "52257-1400",
"dosage_form": "STICK",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TITANIUM DIOXIDE",
"proprietary_name": "ATOMY DERMA CALMING SUN",
"active_ingred_unit": "g/16g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Titanium Dioxide",
"start_marketing_date": "20210501",
"active_numerator_strength": "1.41"
}Access this data programmatically
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