Proven Personalized Day Moisturizer Sunscreen SPF 30

UNIISPL

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

Identification

ManufacturerProven Skincare

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7357200801
30 mL in 1 BOTTLE, PLASTIC (73572-008-01)

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": {
    "5275d2c5-96e8-424d-a3c8-feea778191e4": {
      "match": "brand_token",
      "title": "PROVEN PERSONALIZED DAY MOISTURIZER SUNSCREEN SPF 30 (ZINC OXIDE) CREAM [PROVEN SKINCARE]",
      "spl_version": "3",
      "published_date": "2025-06-23"
    }
  },
  "productid": "73572-008_3804bef6-27b0-89ba-e063-6394a90a5f2f",
  "productndc": "73572-008",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Proven Personalized Day Moisturizer Sunscreen SPF 30",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20250101",
  "active_numerator_strength": "175"
}

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