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United States · US · US:68479-807_1c40d9aa-8e05-4c31-aec4-882f0662f458
Clearing Defense SPF 30
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDermalogica, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1168479807002 mL in 1 POUCH (68479-807-00)
- ndc11684798070115 mL in 1 TUBE (68479-807-01)
- ndc1168479807021 TUBE in 1 CARTON (68479-807-02) / 59 mL in 1 TUBE
- ndc1168479807037 mL in 1 TUBE (68479-807-03)
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": {
"2388ae53-0a61-43c0-8936-c639887a5649": {
"match": "brand_token",
"title": "CLEARING DEFENSE SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE) LOTION [DERMALOGICA, INC.]",
"spl_version": "4",
"published_date": "2025-01-01"
}
},
"productid": "68479-807_1c40d9aa-8e05-4c31-aec4-882f0662f458",
"productndc": "68479-807",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "Clearing Defense SPF 30",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Avobenzone, Homosalate, Octisalate, and Octocrylene",
"start_marketing_date": "20201201",
"active_numerator_strength": "30; 80; 50; 80"
}Access this data programmatically
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