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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

  • ndc11
    3766229661
    200 PELLET in 1 VIAL, GLASS (37662-2966-1)
  • ndc11
    3766229662
    1200 PELLET in 1 BOTTLE, GLASS (37662-2966-2)
  • ndc11
    3766229663
    4000 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"
}

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