Solar Eclipse Extreme Sunscreen

UNIISPL

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

Identification

ManufacturerULTRAVIOLET SKINCARE LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8549120504
113 g in 1 BOTTLE, PUMP (85491-205-04)

Annotations

UNII (FDA Substance ID)

SOI2LOH54Z

ZINC OXIDE

RxCUI 11423

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "SOI2LOH54Z",
    "rxcui": "11423",
    "inchikey": "RNWHGQJWIACOKP-UHFFFAOYSA-N",
    "display_name": "ZINC OXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "4fc170dd-7c6b-b810-e063-6394a90ae61f": {
      "match": "brand_token",
      "title": "SOLAR FLARE SUNLIT HOLIDAY HAND SANITIZERS (GOLDEN CARAMEL, VANILLA SOLSTICE, AMBER ROSE) (ALCOHOL SPRAY) SPRAY [SCENT THEORY PRODUCTS LLC]",
      "spl_version": "1",
      "published_date": "2026-04-22"
    }
  },
  "productid": "85491-205_4614829b-e8c2-c720-e063-6394a90ac40a",
  "productndc": "85491-205",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Solar Eclipse Extreme Sunscreen",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20250514",
  "active_numerator_strength": "200"
}

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