Clear Path Tinted Facial Sunscreen

UNIISPL

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

Identification

ManufacturerLULUS SPA BOUTIQUE

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8573520350
53 g in 1 BOTTLE, PUMP (85735-203-50)

Annotations

UNII (FDA Substance ID)

15FIX9V2JP

TITANIUM DIOXIDE

RxCUI 38323

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "15FIX9V2JP",
    "rxcui": "38323",
    "inchikey": "SOQBVABWOPYFQZ-UHFFFAOYSA-N",
    "display_name": "TITANIUM DIOXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "5bcf01d8-ddf3-4e64-8d3f-3526a51a5859": {
      "match": "brand_token",
      "title": "CLEAR LAX (POLYETHYLENE GLYCOL 3350) POWDER, FOR SOLUTION [HYVEE INC]",
      "spl_version": "6",
      "published_date": "2026-05-13"
    }
  },
  "productid": "85735-203_45782d26-5b24-6cbe-e063-6294a90a4759",
  "productndc": "85735-203",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Clear Path Tinted Facial Sunscreen",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium Dioxide, Zinc Oxide",
  "start_marketing_date": "20180424",
  "active_numerator_strength": "80; 38"
}

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