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United States · US · US:55758-418_1ddc7cb3-05e6-6453-e063-6294a90a620a
Dr. Fibra
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPharmadel LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11557584181010 PACKET in 1 BOX (55758-418-10) / 1 POWDER in 1 PACKET
Annotations
UNII (FDA Substance ID)
0SHO53407G
PSYLLIUM HUSK
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0SHO53407G",
"rxcui": null,
"inchikey": null,
"display_name": "PSYLLIUM HUSK",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"6c5adc3c-9d45-449a-ad42-f9571851cd18": {
"match": "brand_token",
"title": "DR. JOHNE SKIN TAG REMOVER (SALICYLIC ACID) SOLUTION [DR.JOHNES LLC]",
"spl_version": "9",
"published_date": "2026-05-28"
}
},
"productid": "55758-418_1ddc7cb3-05e6-6453-e063-6294a90a620a",
"productndc": "55758-418",
"dosage_form": "POWDER",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "PSYLLIUM HUSK",
"proprietary_name": "Dr. Fibra",
"active_ingred_unit": "g/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Psyllium Husk",
"start_marketing_date": "20240630",
"active_numerator_strength": "3.4"
}Access this data programmatically
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