Titanium Oxydatum

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766229711
200 PELLET in 1 VIAL, GLASS (37662-2971-1)
ndc11
3766229712
500 PELLET in 1 VIAL, GLASS (37662-2971-2)
ndc11
3766229713
3000 PELLET in 1 BOTTLE, GLASS (37662-2971-3)
ndc11
3766229714
10000 PELLET in 1 BOTTLE, GLASS (37662-2971-4)

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": "37662-2971_f9bcf569-7aa5-a0dd-e053-6394a90aeae1",
  "productndc": "37662-2971",
  "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": "500"
}

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