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United States · US · US:0220-1541_0a0c373a-4961-0591-e063-6294a90a8983
Corallium rubrum
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBoiron
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1102201541415 [hp_C] in 1 TUBE (0220-1541-41)
Annotations
UNII (FDA Substance ID)
2CA71K0DLE
CORALLIUM RUBRUM EXOSKELETON
RxCUI 1311193
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2CA71K0DLE",
"rxcui": "1311193",
"inchikey": null,
"display_name": "CORALLIUM RUBRUM EXOSKELETON",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"7a2d4904-d2b1-ef74-e053-2a91aa0a284a": {
"match": "brand_token",
"title": "CORALLIUM RUBRUM (CORALLIUM RUBRUM EXOSKELETON) PELLET [BOIRON]",
"spl_version": "3",
"published_date": "2023-11-14"
}
},
"productid": "0220-1541_0a0c373a-4961-0591-e063-6294a90a8983",
"productndc": "0220-1541",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CORALLIUM RUBRUM EXOSKELETON",
"proprietary_name": "Corallium rubrum",
"active_ingred_unit": "[hp_C]/5[hp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "CORALLIUM RUBRUM EXOSKELETON",
"start_marketing_date": "19830303",
"active_numerator_strength": "5"
}Access this data programmatically
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