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United States · US · US:73572-007_09cc9eb2-c5b1-d6fa-e063-6394a90a4ea2

Personalized Day Moisturizer with SPF 50

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerProven Skincare
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7357200701
    30 mL in 1 BOTTLE (73572-007-01)

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": {
    "d3cf8f81-d6ae-4570-ad86-43415e973e13": {
      "match": "brand_token",
      "title": "PERSONALIZED MOISTURIZER SPF 30 (ZINC OXIDE 10.00%) LOTION [PROVEN SKINCARE]",
      "spl_version": "2",
      "published_date": "2025-12-09"
    }
  },
  "productid": "73572-007_09cc9eb2-c5b1-d6fa-e063-6394a90a4ea2",
  "productndc": "73572-007",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Personalized Day Moisturizer with SPF 50",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20220301",
  "active_numerator_strength": "120"
}

Access this data programmatically

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