Purito Sunday Adventure Sunscreen SPF 50, 50 mL

UNIISPL

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

Identification

ManufacturerHinature

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
7325101001
50 mL in 1 TUBE (73251-010-01)
ndc11
7325101002
1 TUBE in 1 PACKAGE (73251-010-02) / 60 mL in 1 TUBE

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": {
    "bf16f535-97fc-4fd8-9310-8b6bbc82baae": {
      "match": "brand_token",
      "title": "PURITO SUNDAY ADVENTURE SUNSCREEN SPF 50, 50 ML (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM [HINATURE]",
      "spl_version": "7",
      "published_date": "2026-04-09"
    }
  },
  "productid": "73251-010_4e5656c1-3867-9f19-e063-6394a90ab7c8",
  "productndc": "73251-010",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "Purito Sunday Adventure Sunscreen SPF 50, 50 mL",
  "active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE",
  "start_marketing_date": "20250215",
  "active_numerator_strength": "30; 90; 45; 50"
}

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