LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN

UNIISPL

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

Identification

ManufacturerLather, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7739420303
88 mL in 1 TUBE (77394-203-03)

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": {
    "3158a2d7-0db5-f5bf-e063-6294a90a3126": {
      "match": "brand_token",
      "title": "LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN (ZINC OXIDE) CREAM [LATHER, INC.]",
      "spl_version": "2",
      "published_date": "2025-11-17"
    }
  },
  "productid": "77394-203_4135b305-af4e-c673-e063-6394a90aae20",
  "productndc": "77394-203",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20250501",
  "active_numerator_strength": "21"
}

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