Derma E Sun Protection Mineral

UNIISPL

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

Identification

Manufacturerderma e

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5410814861
1 BOTTLE, WITH APPLICATOR in 1 BOX (54108-1486-1) / 5 g in 1 BOTTLE, WITH APPLICATOR

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": {
    "ba38a43d-7a8a-4814-ba34-0e99124f5fca": {
      "match": "brand_token",
      "title": "DERMA B EVERYDAY FIT SUNSCREEN SPF 50 (AVOBEZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [NEOPHARM CO., LTD.]",
      "spl_version": "2",
      "published_date": "2026-02-06"
    }
  },
  "productid": "54108-1486_6b91329e-7dde-4226-8521-7f3c417a8b9e",
  "productndc": "54108-1486",
  "dosage_form": "POWDER",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Derma E Sun Protection Mineral",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc oxide",
  "start_marketing_date": "20240226",
  "active_numerator_strength": "241"
}

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