Dr Lift SPF 50 Mineral Sunscreen Stick

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
6806283141
15 g in 1 TUBE (68062-8314-1)

Annotations

UNII (FDA Substance ID)

SOI2LOH54Z

ZINC OXIDE

RxCUI 11423

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "SOI2LOH54Z",
    "rxcui": "11423",
    "inchikey": "RNWHGQJWIACOKP-UHFFFAOYSA-N",
    "display_name": "ZINC OXIDE",
    "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": "68062-8314_436fdf4f-11da-7c5b-e063-6294a90a8731",
  "productndc": "68062-8314",
  "dosage_form": "STICK",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Dr Lift SPF 50 Mineral Sunscreen Stick",
  "active_ingred_unit": "g/15g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20251112",
  "active_numerator_strength": "3.75"
}

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