Silicea

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
3766220901
80 PELLET in 1 VIAL, GLASS (37662-2090-1)
ndc11
3766220902
200 PELLET in 1 VIAL, GLASS (37662-2090-2)
ndc11
3766220903
1200 PELLET in 1 BOTTLE, GLASS (37662-2090-3)
ndc11
3766220904
4000 PELLET in 1 BOTTLE, GLASS (37662-2090-4)

Annotations

UNII (FDA Substance ID)

ETJ7Z6XBU4

SILICON DIOXIDE

RxCUI 9771

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "ETJ7Z6XBU4",
    "rxcui": "9771",
    "inchikey": "VYPSYNLAJGMNEJ-UHFFFAOYSA-N",
    "display_name": "SILICON DIOXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "a2a1eae8-24c8-44dd-9b9d-1826fa716433": {
      "match": "brand_token",
      "title": "SILICEA 8012 (SILICEA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-2090_efcdc393-5dac-38d1-e053-2995a90acb2e",
  "productndc": "37662-2090",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SILICON DIOXIDE",
  "proprietary_name": "Silicea",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Silicea",
  "start_marketing_date": "20221214",
  "active_numerator_strength": "30"
}

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