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United States Β· US Β· US:83326-002_65123dc9-9354-4015-8507-d8d4e6bc2e01

Zealios SPF LipGuard

UNIISPL

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

Identification

ManufacturerPersonal Best Products Inc. dba Zealios
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    8332600201
    7.39 mL in 1 TUBE, WITH APPLICATOR (83326-002-01)

Annotations

UNII (FDA Substance ID)
G63QQF2NOX
AVOBENZONE
RxCUI 45045
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "G63QQF2NOX",
    "rxcui": "45045",
    "inchikey": "XNEFYCZVKIDDMS-UHFFFAOYSA-N",
    "display_name": "AVOBENZONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "020bd1b4-da50-4117-a4f3-b74aa4187396": {
      "match": "brand_token",
      "title": "ZEALIOS SPORT PERFORMANCE ULTRALIGHT SPF 50 SUNSCREEN (HOMOSALATE, OCTOCRYLENE, OCTISALATE, AND AVOBENZONE) CREAM [PERSONAL BEST PRODUCTS INC. DBA ZEALIOS]",
      "spl_version": "1",
      "published_date": "2026-02-06"
    }
  },
  "productid": "83326-002_65123dc9-9354-4015-8507-d8d4e6bc2e01",
  "productndc": "83326-002",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; OCTISALATE",
  "proprietary_name": "Zealios SPF LipGuard",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "OCTISALATE and AVOBENZONE",
  "start_marketing_date": "20210621",
  "active_numerator_strength": "30; 50"
}

Access this data programmatically

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Zealios SPF LipGuard (US) β€” Drug Database