111 SKIN SUNSCREEN SPF 50

UNIISPL

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

Identification

ManufacturerBentley Laboratories, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
5411119001
1 BOTTLE, PUMP in 1 CARTON (54111-190-01) / 50 mL in 1 BOTTLE, PUMP
ndc11
5411119002
1 BOTTLE, PUMP in 1 CARTON (54111-190-02) / 15 mL in 1 BOTTLE, PUMP

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": {
    "b1265797-71dd-4302-ab26-dbff6ccec856": {
      "match": "brand_token",
      "title": "111 SKIN SUNSCREEN SPF 50 (ZINC OXIDE) SOLUTION [BENTLEY LABORATORIES, LLC]",
      "spl_version": "2",
      "published_date": "2026-01-26"
    }
  },
  "productid": "54111-190_3885e519-7eb8-4b06-97fe-85471b0e6951",
  "productndc": "54111-190",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "111 SKIN SUNSCREEN SPF 50",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20250523",
  "active_numerator_strength": "19.5"
}

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