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United States · US · US:37662-3551_ffdbdb70-8667-f0c6-e053-6394a90a6596
Alumina
UNIISPLATC D10AX04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeD10AX04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc113766235511200 PELLET in 1 VIAL, GLASS (37662-3551-1)
- ndc113766235512500 PELLET in 1 VIAL, GLASS (37662-3551-2)
- ndc1137662355133000 PELLET in 1 BOTTLE, GLASS (37662-3551-3)
- ndc11376623551410000 PELLET in 1 BOTTLE, GLASS (37662-3551-4)
Annotations
UNII (FDA Substance ID)
LMI26O6933
ALUMINUM OXIDE
RxCUI 615
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "LMI26O6933",
"rxcui": "615",
"inchikey": "PNEYBMLMFCGWSK-UHFFFAOYSA-N",
"display_name": "ALUMINUM OXIDE",
"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": "37662-3551_ffdbdb70-8667-f0c6-e053-6394a90a6596",
"productndc": "37662-3551",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALUMINUM OXIDE",
"proprietary_name": "Alumina",
"active_ingred_unit": "[hp_M]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Alumina",
"start_marketing_date": "20230706",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code D10AX04.
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