Botnia Gentle Sun SPF 30

UNIISPL

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

Identification

ManufacturerBotnia, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8746190400
1 TUBE in 1 BOX (87461-904-00) / 50 mL in 1 TUBE

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": {
    "005d0245-fe53-47e5-888b-683f58cd6d26": {
      "match": "brand_token",
      "title": "BOTNIA GENTLE SUN SPF 30 (ZINC OXIDE) CREAM [BOTNIA, INC]",
      "spl_version": "1",
      "published_date": "2026-03-05"
    }
  },
  "productid": "87461-904_4c1e721a-a8f5-db1b-e063-6294a90a0a26",
  "productndc": "87461-904",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Botnia Gentle Sun SPF 30",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20260119",
  "active_numerator_strength": "180"
}

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