SEYTU Body Sunscreen

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerOmnilife USA, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8427100101
1 TUBE in 1 BOX (84271-001-01) / 120 mL in 1 TUBE

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": {
    "c411e9a6-b2ea-446b-a886-b92c61736e6c": {
      "match": "brand_token",
      "title": "SEYTU BODY SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [OMNILIFE USA, INC.]",
      "spl_version": "2",
      "published_date": "2026-02-06"
    }
  },
  "productid": "84271-001_1959d76a-87e7-4cdd-9f18-40635e23e2a7",
  "productndc": "84271-001",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "SEYTU Body Sunscreen",
  "active_ingred_unit": "g/100mL; g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "titanium dioxide and zinc oxide",
  "start_marketing_date": "20240415",
  "active_numerator_strength": "8.3; 4.875"
}

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