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United States Β· US Β· US:85752-208_45b366af-ed2e-dd34-e063-6394a90affbd

GLOW UP Ageless Daily Protection Sunscreen

UNIISPL

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

Identification

ManufacturerCLEAN SLATE SKIN & BODY, INC.
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    8575220850
    50 g in 1 BOTTLE, PUMP (85752-208-50)

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": {
    "4619cf96-987a-3e88-e063-6294a90afbe9": {
      "match": "brand_token",
      "title": "GLOW THIS WAY (OCTISALATE, OCTOCRYLENE, ZINC OXIDE, AVOBENZONE, HOMOSALATE) KIT [KOCO LIFE LLC]",
      "spl_version": "1",
      "published_date": "2026-02-18"
    }
  },
  "productid": "85752-208_45b366af-ed2e-dd34-e063-6394a90affbd",
  "productndc": "85752-208",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "GLOW UP Ageless Daily Protection Sunscreen",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20210415",
  "active_numerator_strength": "160"
}

Access this data programmatically

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GLOW UP Ageless Daily Protection Sunscreen (US) β€” Drug Database