Solarium Daily Essentials Luminizing Glow Drops

UNIISPL

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

Identification

ManufacturerSolarium Brands LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8489121911
30 mL in 1 TUBE (84891-2191-1)

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": {
    "302a4efe-d429-b1c4-e063-6294a90a073d": {
      "match": "brand_token",
      "title": "SOLARIUM DAILY ESSENTIALS LUMINIZING GLOW DROPS (ZINC OXIDE) LOTION [SOLARIUM BRANDS LLC]",
      "spl_version": "3",
      "published_date": "2025-11-18"
    }
  },
  "productid": "84891-2191_43cc8ed8-24ef-87bb-e063-6394a90a5f8f",
  "productndc": "84891-2191",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Solarium Daily Essentials Luminizing Glow Drops",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20241220",
  "active_numerator_strength": "132"
}

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