Amnion Oxalis comp.

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
4895113963
60 mL in 1 BOTTLE, DROPPER (48951-1396-3)

Annotations

UNII (FDA Substance ID)

P06X62O7E9

AMNIOTIC FLUID (BOVINE)

RxCUI 1368127

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "P06X62O7E9",
    "rxcui": "1368127",
    "inchikey": null,
    "display_name": "AMNIOTIC FLUID (BOVINE)",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "2d63d8f2-db97-43ab-addd-e6be61a66e01": {
      "match": "brand_token",
      "title": "AMNION 30 LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "5",
      "published_date": "2025-11-27"
    }
  },
  "productid": "48951-1396_2d7f3585-002c-854b-e063-6294a90ab9fa",
  "productndc": "48951-1396",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AMNIOTIC FLUID (BOVINE); KALANCHOE DAIGREMONTIANA LEAF; OXALIS STRICTA WHOLE",
  "proprietary_name": "Amnion Oxalis comp.",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Amnion Oxalis comp.",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "30; 3; 3"
}

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