Sun Pyrite 8X

UNIISPL

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

Identification

ManufacturerUriel Pharmacy, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4895184334
50 g in 1 BOTTLE (48951-8433-4)

Annotations

UNII (FDA Substance ID)

132N09W4PR

FERROUS DISULFIDE

RxCUI 1544140

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "132N09W4PR",
    "rxcui": "1544140",
    "inchikey": "NIFIFKQPDTWWGU-UHFFFAOYSA-N",
    "display_name": "FERROUS DISULFIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "522fc8a4-ce9f-8be8-e063-6294a90aebf0": {
      "match": "brand_token",
      "title": "SUN BUM AMAZON 8 OZ SPF 70 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION SUN BUM AMAZON 8 OZ SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION SUN BUM AMAZON 8 OZ SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION SUN BUM AMAZON 8 OZ SPF 15 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [SUN BUM]",
      "spl_version": "1",
      "published_date": "2026-05-21"
    }
  },
  "productid": "48951-8433_2eae3f2d-b712-0f50-e063-6294a90a8349",
  "productndc": "48951-8433",
  "dosage_form": "POWDER",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FERROUS DISULFIDE",
  "proprietary_name": "Sun Pyrite 8X",
  "active_ingred_unit": "[hp_X]/g",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Sun Pyrite 8X",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "8"
}

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