Bondi Sands SPF 60 Sunny Drops Face Serum

UNIISPL

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

Identification

ManufacturerBONDI SANDS (USA) INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7995002101
1 TUBE in 1 CARTON (79950-021-01) / 30 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": {
    "2861453a-12e9-faeb-e063-6394a90a527c": {
      "match": "brand_token",
      "title": "BONDI SANDS BROAD SPECTRUM SPF 60 SUNNY CREAM BODY (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BAXTER LABORATORIES PTY. LTD.]",
      "spl_version": "2",
      "published_date": "2025-11-17"
    }
  },
  "productid": "79950-021_2b5bd2d9-749a-b81b-e063-6394a90ad5bc",
  "productndc": "79950-021",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "Bondi Sands SPF 60 Sunny Drops Face Serum",
  "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": "20250110",
  "active_numerator_strength": "30; 120; 50; 100"
}

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