78 x 36 SPF 30 Active

UNIISPL

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

Identification

ManufacturerDermazone LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5846610903
1 TUBE in 1 CARTON (58466-109-03) / 96 g 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": {
    "96a8aacc-5c2f-410a-8fb4-8b3bc0f81e55": {
      "match": "brand_token",
      "title": "78 X 36 SPF 30 ACTIVE (ZINC OXIDE) CREAM [DERMAZONE LLC]",
      "spl_version": "2",
      "published_date": "2025-07-28"
    }
  },
  "productid": "58466-109_1c2b73fd-1c52-4db3-982e-d937c04ceeac",
  "productndc": "58466-109",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "78 x 36 SPF 30 Active",
  "active_ingred_unit": "g/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20231001",
  "active_numerator_strength": ".2"
}

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