Avail Facial Sunscreen SPF 25

UNIISPL

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

Identification

ManufacturerEmeis Cosmetics Pty Ltd

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
7629305501
1 BOTTLE, PUMP in 1 CARTON (76293-055-01) / 50.8 g in 1 BOTTLE, PUMP
ndc11
7629305502
1 BOTTLE, PUMP in 1 CARTON (76293-055-02) / 5 g in 1 BOTTLE, PUMP

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": {
    "7be903e4-5f07-35b2-e053-2991aa0a1340": {
      "match": "brand_token",
      "title": "AVAIL FACIAL SUNSCREEN SPF 25 (HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE) LOTION [EMEIS COSMETICS PTY LTD]",
      "spl_version": "4",
      "published_date": "2025-12-19"
    }
  },
  "productid": "76293-055_1796b70e-f34f-474e-8ea2-3a35512a7fd8",
  "productndc": "76293-055",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "Avail Facial Sunscreen SPF 25",
  "active_ingred_unit": "mg/g; mg/g; mg/g; mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Homosalate, Octocrylene, Octisalate, Avobenzone",
  "start_marketing_date": "20190101",
  "active_numerator_strength": "30; 90; 40; 70"
}

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