Antioxidant SPF

UNIISPL

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

Identification

ManufacturerTeton Dermatology Holdings, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8533920850
50 g in 1 BOTTLE, PUMP (85339-208-50)

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": {
    "37dc70ba-a6bb-fe09-e063-6394a90a5129": {
      "match": "brand_token",
      "title": "ANTIOXIDANT MINERAL SUNSCREEN PLUS PRIMER LIGHTLY TINTED (ZINC OXIDE) CREAM [TRUE BEAUTY BROWS & SKIN CARE]",
      "spl_version": "2",
      "published_date": "2025-12-16"
    }
  },
  "productid": "85339-208_45b3a6e6-720c-2308-e063-6294a90ace4f",
  "productndc": "85339-208",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Antioxidant SPF",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20231027",
  "active_numerator_strength": "160"
}

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