Dr Loretta Universal Glow Daily Defense SPF 40

UNIISPL

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

Identification

ManufacturerDr. Loretta, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
7150119101
1.5 mL in 1 PACKET (71501-1910-1)
ndc11
7150119102
100 mL in 1 BOTTLE, PUMP (71501-1910-2)
ndc11
7150119103
1 BOTTLE, PUMP in 1 BOX (71501-1910-3) / 10 mL in 1 BOTTLE, PUMP

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": "71501-1910_47cc5bc2-c2d5-d1a4-e063-6294a90a5dc8",
  "productndc": "71501-1910",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Dr Loretta Universal Glow Daily Defense SPF 40",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20250901",
  "active_numerator_strength": "170"
}

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