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United States · US · US:52257-1430_ae120587-f224-476d-9b7a-b3df395b7cbf

ATOMY BB SUNSCREEN

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

  • ndc11
    5225714301
    40 mL in 1 CARTON (52257-1430-1)

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": "52257-1430_ae120587-f224-476d-9b7a-b3df395b7cbf",
  "productndc": "52257-1430",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "ATOMY BB SUNSCREEN",
  "active_ingred_unit": "g/100mL; g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium Dioxide, Zinc Oxide",
  "start_marketing_date": "20231001",
  "active_numerator_strength": "8.22; 5.76"
}

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