Chromium Sulphuricum

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
3766202861
200 PELLET in 1 VIAL, GLASS (37662-0286-1)
ndc11
3766202862
500 PELLET in 1 VIAL, GLASS (37662-0286-2)
ndc11
3766202863
3000 PELLET in 1 BOTTLE, GLASS (37662-0286-3)
ndc11
3766202864
10000 PELLET in 1 BOTTLE, GLASS (37662-0286-4)

Annotations

UNII (FDA Substance ID)

Y0C99N5TMZ

CHROMIC SULFATE

RxCUI 90402

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "Y0C99N5TMZ",
    "rxcui": "90402",
    "inchikey": "GRWVQDDAKZFPFI-UHFFFAOYSA-H",
    "display_name": "CHROMIC SULFATE",
    "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": "37662-0286_e07d8748-7d6c-0d84-e053-2a95a90ad536",
  "productndc": "37662-0286",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CHROMIC SULFATE",
  "proprietary_name": "Chromium Sulphuricum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Chromium Sulphuricum",
  "start_marketing_date": "20220602",
  "active_numerator_strength": "100"
}

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