Badger Broad Spectrum SPF 35 Active Face Stick

UNIISPL

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

Identification

ManufacturerW.S. Badger Company, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6220635322
18.4 g in 1 APPLICATOR (62206-3532-2)

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": {
    "2a96c423-f4ad-0f07-e063-6394a90a39f8": {
      "match": "brand_token",
      "title": "BADGER SPF 50 ADVENTURE SPORT MINERAL SUNSCREEN CREAM (ZINC OXIDE) CREAM [W.S. BADGER COMPANY, INC.]",
      "spl_version": "3",
      "published_date": "2026-04-09"
    }
  },
  "productid": "62206-3532_2a93f206-b354-37d0-e063-6394a90a4ee2",
  "productndc": "62206-3532",
  "dosage_form": "STICK",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Badger Broad Spectrum SPF 35 Active Face Stick",
  "active_ingred_unit": "g/100g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20220101",
  "active_numerator_strength": "22.5"
}

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