Phosphorus

UNIISPL

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

Identification

ManufacturerEnergique, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4491101751
30 mL in 1 BOTTLE, DROPPER (44911-0175-1)

Annotations

UNII (FDA Substance ID)

27YLU75U4W

PHOSPHORUS

RxCUI 8263

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "27YLU75U4W",
    "rxcui": "8263",
    "inchikey": "OAICVXFJPJFONN-UHFFFAOYSA-N",
    "display_name": "PHOSPHORUS",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "01ebfc7a-d7d5-4003-ac57-da5ba242931a": {
      "match": "brand_token",
      "title": "PHOSPHORUS 30 LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "4",
      "published_date": "2026-02-26"
    }
  },
  "productid": "44911-0175_19c16b14-a9b9-4ad9-97ca-efcf5d58fc9a",
  "productndc": "44911-0175",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PHOSPHORUS",
  "proprietary_name": "Phosphorus",
  "active_ingred_unit": "[hp_C]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Phosphorus",
  "start_marketing_date": "20150707",
  "active_numerator_strength": "200"
}

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