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United States · US · US:58264-0385_2b531e4a-4cbe-7089-e063-6394a90ae44f
G-22
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDNA Labs, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11582640385259.14 mL in 1 BOTTLE, GLASS (58264-0385-2)
Annotations
UNII (FDA Substance ID)
FC604DJ98E
LIGUSTRUM VULGARE WHOLE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "FC604DJ98E",
"rxcui": null,
"inchikey": null,
"display_name": "LIGUSTRUM VULGARE WHOLE",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "SUBLINGUAL",
"spl_meta": {
"d30d72f9-458d-4daa-8481-6cae8ad49b9f": {
"match": "brand_token",
"title": "G-22 (LIGUSTRUM VULGARE WHOLE) SOLUTION [DNA LABS, INC.]",
"spl_version": "3",
"published_date": "2025-01-13"
}
},
"productid": "58264-0385_2b531e4a-4cbe-7089-e063-6394a90ae44f",
"productndc": "58264-0385",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LIGUSTRUM VULGARE WHOLE",
"proprietary_name": "G-22",
"active_ingred_unit": "[hp_X]/mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "LIGUSTRUM VULGARE WHOLE",
"start_marketing_date": "19900101",
"active_numerator_strength": "1"
}Access this data programmatically
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