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United States · US · US:37662-2966_f9bcf569-7aa5-a0dd-e053-6394a90aeae1
Titanium Oxydatum
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc113766229661200 PELLET in 1 VIAL, GLASS (37662-2966-1)
- ndc1137662296621200 PELLET in 1 BOTTLE, GLASS (37662-2966-2)
- ndc1137662296634000 PELLET in 1 BOTTLE, GLASS (37662-2966-3)
Annotations
UNII (FDA Substance ID)
6XWR967CBZ
TITANIUM OXYSULFATE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "6XWR967CBZ",
"rxcui": null,
"inchikey": "DCKVFVYPWDKYDN-UHFFFAOYSA-L",
"display_name": "TITANIUM OXYSULFATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"36c57e6f-c747-9926-e063-6294a90a5721": {
"match": "brand_token",
"title": "TITANIUM DIOXIDE, ZINC OXIDE (ON THE GO SUNSCREEN STICK) STICK [REVIVE IN SOLANO]",
"spl_version": "2",
"published_date": "2025-12-16"
}
},
"productid": "37662-2966_f9bcf569-7aa5-a0dd-e053-6394a90aeae1",
"productndc": "37662-2966",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TITANIUM OXYSULFATE",
"proprietary_name": "Titanium Oxydatum",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Titanium Oxydatum",
"start_marketing_date": "20230419",
"active_numerator_strength": "6"
}Access this data programmatically
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