Dr Lift Mineral SPF 30

UNIISPL

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

Identification

ManufacturerSpa de Soleil

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6806283121
100 mL in 1 BOTTLE, SPRAY (68062-8312-1)

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": {
    "8abd6d8e-c69e-4374-ace8-d42b2d3e171e": {
      "match": "brand_token",
      "title": "DR SCHOLLS FUNGAL NAIL CLEAR AND CURE TOLNAFTATE ANTIFUNGAL (TOLNAFTATE) LIQUID [SCHOLL'S WELLNESS COMPANY LLC]",
      "spl_version": "4",
      "published_date": "2026-05-20"
    }
  },
  "productid": "68062-8312_40c0e413-70f6-25c9-e063-6294a90ad27d",
  "productndc": "68062-8312",
  "dosage_form": "SPRAY",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE",
  "proprietary_name": "Dr Lift Mineral SPF 30",
  "active_ingred_unit": "mg/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "titanium dioxide",
  "start_marketing_date": "20251009",
  "active_numerator_strength": "72"
}

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