Brickell Mens Products Daily Defense Face Moisturizer SPF-20

UNIISPL

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

Identification

ManufacturerBRICKELL BRANDS LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8224742100
100 mL in 1 TUBE (82247-421-00)

Annotations

UNII (FDA Substance ID)

4X49Y0596W

OCTISALATE

RxCUI 91327

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4X49Y0596W",
    "rxcui": "91327",
    "inchikey": "FMRHJJZUHUTGKE-UHFFFAOYSA-N",
    "display_name": "OCTISALATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "7ba3b13b-cb78-4df8-8719-c88e556643b4": {
      "match": "brand_token",
      "title": "BRICKELL MENS PRODUCTS RELIEVING ANTI-DANDRUFF (SALICYLIC ACID) LIQUID [BRICKELL BRANDS LLC]",
      "spl_version": "1",
      "published_date": "2025-06-17"
    }
  },
  "productid": "82247-421_09e30a62-358f-3cff-e063-6394a90a270f",
  "productndc": "82247-421",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTISALATE; ZINC OXIDE",
  "proprietary_name": "Brickell Mens Products Daily Defense Face Moisturizer SPF-20",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "OCTISALATE, ZINC OXIDE",
  "start_marketing_date": "20230911",
  "active_numerator_strength": "50; 40"
}

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