Knesko Skin The Sunscreen

UNIISPL

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

Identification

ManufacturerKnesko, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8740723602
1 BOTTLE in 1 CARTON (87407-236-02) / 50 mL in 1 BOTTLE (87407-236-01)

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": {
    "5114dc75-a865-326e-e063-6294a90a8911": {
      "match": "brand_token",
      "title": "KNESKO SKIN THE SUNSCREEN (ZINC OXIDE) LOTION [KNESKO, LLC]",
      "spl_version": "1",
      "published_date": "2026-05-11"
    }
  },
  "productid": "87407-236_5114ef81-229c-690c-e063-6394a90a0cd0",
  "productndc": "87407-236",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Knesko Skin The Sunscreen",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20260420",
  "active_numerator_strength": "132"
}

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