PORESCREEN SPF40

UNIISPL

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

Identification

ManufacturerDermalogica, LLC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
6847929102
1 TUBE in 1 CARTON (68479-291-02) / 30 mL in 1 TUBE
ndc11
6847929104
59 mL in 1 TUBE (68479-291-04)
ndc11
6847929105
5 mL in 1 TUBE (68479-291-05)

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": {
    "37a7362a-b251-4d3a-a957-65d8f338fa12": {
      "match": "brand_token",
      "title": "PORESCREEN SPF40 (ZINC OXIDE) LOTION [DERMALOGICA, LLC.]",
      "spl_version": "4",
      "published_date": "2025-01-01"
    }
  },
  "productid": "68479-291_67812343-d9bc-43df-88d2-85adf578604e",
  "productndc": "68479-291",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "PORESCREEN SPF40",
  "active_ingred_unit": "mg/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20221201",
  "active_numerator_strength": "10"
}

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