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United States · US · US:41520-515_3a3f3022-318e-1a2c-e063-6394a90ab501
CAREONE
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerFOODHOLD USA
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc114152051514660 g in 1 BOTTLE, PLASTIC (41520-515-14)
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": {
"206f5483-7de1-4bc3-af27-190e211bcb95": {
"match": "brand_token",
"title": "CAREONE ACID RELIEF (FAMOTIDINE) TABLET, FILM COATED [AMERICAN SALES COMPANY]",
"spl_version": "9",
"published_date": "2026-05-25"
}
},
"productid": "41520-515_3a3f3022-318e-1a2c-e063-6394a90ab501",
"productndc": "41520-515",
"dosage_form": "POWDER",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "PSYLLIUM HUSK",
"proprietary_name": "CAREONE",
"active_ingred_unit": "g/5.8g",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Psyllium Husk",
"start_marketing_date": "20190418",
"active_numerator_strength": "3.4"
}Access this data programmatically
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