DreamBeam Sunscreen

UNIISPL

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

Identification

ManufacturerKosas Cosmetics, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8255410240
1 TUBE in 1 BOX (82554-102-40) / 40 mL in 1 TUBE

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": {
    "2e093b82-2a36-cc0f-e063-6394a90a4d6d": {
      "match": "brand_token",
      "title": "DREAMBEAM SUNSCREEN SUNLIT (SUNSCREEN ZINC OXIDE) LOTION [KOSAS COSMETICS, LLC]",
      "spl_version": "3",
      "published_date": "2025-02-17"
    }
  },
  "productid": "82554-102_2e097873-ed14-f306-e063-6394a90a1a48",
  "productndc": "82554-102",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "DreamBeam Sunscreen",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Sunscreen Zinc Oxide",
  "start_marketing_date": "20230414",
  "active_numerator_strength": "21.7"
}

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