Alumina Silicata

UNIISPLATC A07BC02

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC codeA07BC02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766235181
200 PELLET in 1 VIAL, GLASS (37662-3518-1)
ndc11
3766235182
500 PELLET in 1 VIAL, GLASS (37662-3518-2)
ndc11
3766235183
3000 PELLET in 1 BOTTLE, GLASS (37662-3518-3)
ndc11
3766235184
10000 PELLET in 1 BOTTLE, GLASS (37662-3518-4)

Annotations

UNII (FDA Substance ID)

24H4NWX5CO

KAOLIN

RxCUI 6102

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "24H4NWX5CO",
    "rxcui": "6102",
    "inchikey": "KGOIAFZMMLWXLM-UHFFFAOYSA-N",
    "display_name": "KAOLIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "312cac13-2009-4b8f-a09b-9be2d2801df5": {
      "match": "brand_token",
      "title": "ALUMINA COMBINATION 9204 (ALUMINA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-3518_ffc66c2f-d6f9-0fd1-e053-6294a90a4001",
  "productndc": "37662-3518",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "KAOLIN",
  "proprietary_name": "Alumina Silicata",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Alumina Silicata",
  "start_marketing_date": "20230705",
  "active_numerator_strength": "1"
}

Related drugs

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