PHOSPHORUS

UNIISPL

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

Identification

ManufacturerRxhomeo Private Limited d.b.a. Rxhomeo, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
1563103360
100 PELLET in 1 PACKAGE (15631-0336-0)
ndc11
1563103361
200 PELLET in 1 PACKAGE (15631-0336-1)
ndc11
1563103362
400 PELLET in 1 PACKAGE (15631-0336-2)
ndc11
1563103363
750 PELLET in 1 PACKAGE (15631-0336-3)
ndc11
1563103364
2500 PELLET in 1 PACKAGE (15631-0336-4)
ndc11
1563103365
12500 PELLET in 1 PACKAGE (15631-0336-5)
ndc11
1563103366
500 PELLET in 1 PACKAGE (15631-0336-6)
ndc11
1563103367
1000 PELLET in 1 PACKAGE (15631-0336-7)

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": "15631-0336_ca7b6768-4d86-1c6d-e053-2995a90a2319",
  "productndc": "15631-0336",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PHOSPHORUS",
  "proprietary_name": "PHOSPHORUS",
  "active_ingred_unit": "[hp_X]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "PHOSPHORUS",
  "start_marketing_date": "20150912",
  "active_numerator_strength": "4"
}

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