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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

  • ndc11
    6642856700
    1 TUBE in 1 BOX (66428-567-00) / 20 mL in 1 TUBE
  • ndc11
    6642856704
    1 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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