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United States · US · US:37662-2319_f208f88c-3c4e-f177-e053-2995a90aba01
Sulphur
UNIISPLATC D10AB02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeD10AB02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc113766223191200 PELLET in 1 VIAL, GLASS (37662-2319-1)
- ndc113766223192500 PELLET in 1 VIAL, GLASS (37662-2319-2)
- ndc1137662231933000 PELLET in 1 BOTTLE, GLASS (37662-2319-3)
- ndc11376622319410000 PELLET in 1 BOTTLE, GLASS (37662-2319-4)
Annotations
UNII (FDA Substance ID)
70FD1KFU70
SULFUR
RxCUI 10223
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "70FD1KFU70",
"rxcui": "10223",
"inchikey": "JLQNHALFVCURHW-UHFFFAOYSA-N",
"display_name": "SULFUR",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"86939754-cda0-0f13-e053-2a91aa0a399b": {
"match": "brand_token",
"title": "SULPHUR IODATUM (SULFUR IODIDE) PELLET [BOIRON]",
"spl_version": "3",
"published_date": "2026-05-06"
}
},
"productid": "37662-2319_f208f88c-3c4e-f177-e053-2995a90aba01",
"productndc": "37662-2319",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "SULFUR",
"proprietary_name": "Sulphur",
"active_ingred_unit": "[hp_M]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Sulphur",
"start_marketing_date": "20230111",
"active_numerator_strength": "1"
}Related drugs
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