Hybrid SPF

UNIISPL

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

Identification

ManufacturerTopiderm, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5132612801
177 mL in 1 CAN (51326-128-01)

Annotations

UNII (FDA Substance ID)

4X49Y0596W

OCTISALATE

RxCUI 91327

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4X49Y0596W",
    "rxcui": "91327",
    "inchikey": "FMRHJJZUHUTGKE-UHFFFAOYSA-N",
    "display_name": "OCTISALATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "5c99f98c-025c-4886-824f-af968033baf4": {
      "match": "brand_token",
      "title": "HYBRID SPF SPF 30 (OCTOCRYLENE, OCTISALATE, ZINC OXIDE) SPRAY [TOPIDERM, INC.]",
      "spl_version": "2",
      "published_date": "2026-01-23"
    }
  },
  "productid": "51326-128_6e898b78-e4b8-4cad-a2a0-b3b05ebcffab",
  "productndc": "51326-128",
  "dosage_form": "SPRAY",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTISALATE; OCTOCRYLENE; ZINC OXIDE",
  "proprietary_name": "Hybrid SPF",
  "active_ingred_unit": "mg/mL; mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Octocrylene, Octisalate, Zinc Oxide",
  "start_marketing_date": "20241007",
  "active_numerator_strength": "50; 80; 50"
}

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