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United States Β· US Β· US:37662-2698_f49f4a93-d9a7-0964-e053-2995a90a867e
Aluminum Metallicum
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 4
- ndc113766226981200 PELLET in 1 VIAL, GLASS (37662-2698-1)
- ndc113766226982500 PELLET in 1 VIAL, GLASS (37662-2698-2)
- ndc1137662269833000 PELLET in 1 BOTTLE, GLASS (37662-2698-3)
- ndc11376622698410000 PELLET in 1 BOTTLE, GLASS (37662-2698-4)
Annotations
UNII (FDA Substance ID)
CPD4NFA903
ALUMINUM
RxCUI 1311504
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "CPD4NFA903",
"rxcui": "1311504",
"inchikey": "XAGFODPZIPBFFR-UHFFFAOYSA-N",
"display_name": "ALUMINUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"60a54d4e-89c2-4329-86bf-a288527f37b5": {
"match": "brand_token",
"title": "ALUMINUM HYDROXIDE (ALUMINUM HYDROXIDE) LIQUID [ATLANTIC BIOLOGICALS CORP.]",
"spl_version": "7",
"published_date": "2025-12-16"
}
},
"productid": "37662-2698_f49f4a93-d9a7-0964-e053-2995a90a867e",
"productndc": "37662-2698",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALUMINUM",
"proprietary_name": "Aluminum Metallicum",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Aluminum Metallicum",
"start_marketing_date": "20230216",
"active_numerator_strength": "200"
}Access this data programmatically
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