dr. brandt SUN SHIELD SPF 50

UNIISPL

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

Identification

ManufacturerDr. Brandt

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8156810150
1 BOTTLE, DROPPER in 1 BOX (81568-101-50) / 50 mL in 1 BOTTLE, DROPPER

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": {
    "6c5adc3c-9d45-449a-ad42-f9571851cd18": {
      "match": "brand_token",
      "title": "DR. JOHNE SKIN TAG REMOVER (SALICYLIC ACID) SOLUTION [DR.JOHNES LLC]",
      "spl_version": "9",
      "published_date": "2026-05-28"
    }
  },
  "productid": "81568-101_d6922659-fdc4-48c0-a7d6-a3051be051c1",
  "productndc": "81568-101",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "dr. brandt SUN SHIELD SPF 50",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20210215",
  "active_numerator_strength": "17"
}

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