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United States · US · US:66428-567_2740d21d-abbe-c2cc-e063-6294a90ace2c
Theraderm Platinum Protection Facial Sunscreen SPF 40
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTherapon Inc
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1166428567001 TUBE in 1 BOX (66428-567-00) / 20 mL in 1 TUBE
- ndc1166428567041 TUBE in 1 BOX (66428-567-04) / 118 mL in 1 TUBE
Annotations
UNII (FDA Substance ID)
4X49Y0596W
OCTISALATE
RxCUI 91327
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4X49Y0596W",
"rxcui": "91327",
"inchikey": "FMRHJJZUHUTGKE-UHFFFAOYSA-N",
"display_name": "OCTISALATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"1fea6ad8-4d33-4f7c-800c-1bee644bd97f": {
"match": "brand_token",
"title": "THERADERM PLATINUM PROTECTION FACIAL SUNSCREEN SPF 40 (OCTOCRYLENE, OCTISALATE, ZINC OXIDE) LOTION [THERAPON INC]",
"spl_version": "1",
"published_date": "2024-11-21"
}
},
"productid": "66428-567_2740d21d-abbe-c2cc-e063-6294a90ace2c",
"productndc": "66428-567",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTISALATE; OCTOCRYLENE; ZINC OXIDE",
"proprietary_name": "Theraderm Platinum Protection Facial Sunscreen SPF 40",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "OCTOCRYLENE, OCTISALATE, ZINC OXIDE",
"start_marketing_date": "20241101",
"active_numerator_strength": "50; 100; 40"
}Access this data programmatically
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