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United States · US · US:70484-008_37f244fd-c02e-e66a-e063-6394a90aed81

SPF 50 Daily UV Defense Broad Spectrum Sunscreen

UNIISPLATC D02BA

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerVi Medical Products, INC
CountryUS (United States)
ATC codeD02BA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    7048400802
    1 TUBE in 1 CARTON (70484-008-02) / 59 mL in 1 TUBE (70484-008-01)
  • ndc11
    7048400806
    1 TUBE in 1 BOX (70484-008-06) / 22 mL in 1 TUBE (70484-008-05)

Annotations

UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "4Y5P7MUD51",
    "rxcui": "13369",
    "inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
    "display_name": "OCTINOXATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "e97d82fe-cd45-43a5-9c1f-3900025240a1": {
      "match": "brand_token",
      "title": "SPF 50 MINERAL SUNSCREEN FACE AND BODY (ZINC OXIDE) LOTION [TODDLE BORN WILD, INC.]",
      "spl_version": "3",
      "published_date": "2026-05-28"
    }
  },
  "productid": "70484-008_37f244fd-c02e-e66a-e063-6394a90aed81",
  "productndc": "70484-008",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTINOXATE; ZINC OXIDE",
  "proprietary_name": "SPF 50 Daily UV Defense Broad Spectrum Sunscreen",
  "active_ingred_unit": "g/100mL; g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Octinoxate, Zinc Oxide",
  "start_marketing_date": "20250206",
  "active_numerator_strength": "7.5; 10.8"
}

Related drugs

Other records sharing ATC code D02BA.

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