Activated Mineral Sunscreen Tinted

UNIISPL

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

Identification

ManufacturerReve Skincare LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8308300250
1 TUBE in 1 CARTON (83083-002-50) / 50 mL in 1 TUBE

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": {
    "312a32a7-d253-f10c-e063-6294a90a803a": {
      "match": "brand_token",
      "title": "ACTIVATED MINERAL SUNSCREEN TINTED CREAM [REVE SKINCARE LLC]",
      "spl_version": "2",
      "published_date": "2025-12-05"
    }
  },
  "productid": "83083-002_452053bf-8b70-6550-e063-6294a90a23be",
  "productndc": "83083-002",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Activated Mineral Sunscreen Tinted",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Activated Mineral Sunscreen Tinted",
  "start_marketing_date": "20250325",
  "active_numerator_strength": "142.8"
}

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