Chromium Phosphoricum

UNIISPL

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766204311
200 PELLET in 1 VIAL, GLASS (37662-0431-1)
ndc11
3766204312
500 PELLET in 1 VIAL, GLASS (37662-0431-2)
ndc11
3766204313
3000 PELLET in 1 BOTTLE, GLASS (37662-0431-3)
ndc11
3766204314
10000 PELLET in 1 BOTTLE, GLASS (37662-0431-4)

Annotations

UNII (FDA Substance ID)

AQ86ZJ9U98

CHROMIC PHOSPHATE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "AQ86ZJ9U98",
    "rxcui": null,
    "inchikey": "IKZBVTPSNGOVRJ-UHFFFAOYSA-K",
    "display_name": "CHROMIC PHOSPHATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "da207ca8-7836-4c66-92fe-36cc89baf773": {
      "match": "brand_token",
      "title": "CHROMIUM (CHROMIC CHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]",
      "spl_version": "10",
      "published_date": "2026-05-25"
    }
  },
  "productid": "37662-0431_e106918d-3ec7-4c5e-e053-2995a90ab69c",
  "productndc": "37662-0431",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CHROMIC PHOSPHATE",
  "proprietary_name": "Chromium Phosphoricum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Chromium Phosphoricum",
  "start_marketing_date": "20220609",
  "active_numerator_strength": "1"
}

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