Private Label Sunscreen SPF35 40min WR RE126-202

UNIISPL

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

Identification

ManufacturerSwiss-American CDMO, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6023200361
30 g in 1 PACKAGE (60232-0036-1)

Annotations

UNII (FDA Substance ID)

V06SV4M95S

HOMOSALATE

RxCUI 91326

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "V06SV4M95S",
    "rxcui": "91326",
    "inchikey": "WSSJONWNBBTCMG-UHFFFAOYSA-N",
    "display_name": "HOMOSALATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "e74bddea-c1ac-4e4e-84bd-5a9defb85b2d": {
      "match": "brand_token",
      "title": "PRIVATE LABEL ANTIFUNGAL BARRIER CREAM (2% MICONAZOLE NITRATE CREAM) CREAM [SWISS-AMERICAN CDMO, LLC]",
      "spl_version": "4",
      "published_date": "2026-01-09"
    }
  },
  "productid": "60232-0036_fe000ceb-250f-465c-81cf-ed3d78f0e7f4",
  "productndc": "60232-0036",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HOMOSALATE; OCTISALATE; ZINC OXIDE",
  "proprietary_name": "Private Label Sunscreen SPF35 40min WR RE126-202",
  "active_ingred_unit": "g/1000g; g/1000g; g/1000g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "homosalate, zinc oxide sunscreen",
  "start_marketing_date": "20231109",
  "active_numerator_strength": "90; 50; 100"
}

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