Titanium Sulphuratum

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
3766229801
200 PELLET in 1 VIAL, GLASS (37662-2980-1)
ndc11
3766229802
500 PELLET in 1 VIAL, GLASS (37662-2980-2)
ndc11
3766229803
3000 PELLET in 1 BOTTLE, GLASS (37662-2980-3)
ndc11
3766229804
10000 PELLET in 1 BOTTLE, GLASS (37662-2980-4)

Annotations

UNII (FDA Substance ID)

40HP4T69SE

TITANIUM DISULFATE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "40HP4T69SE",
    "rxcui": null,
    "inchikey": "HDUMBHAAKGUHAR-UHFFFAOYSA-J",
    "display_name": "TITANIUM DISULFATE",
    "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": "37662-2980_f9bda25d-2a82-a951-e053-6394a90a8503",
  "productndc": "37662-2980",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DISULFATE",
  "proprietary_name": "Titanium Sulphuratum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Titanium Sulphuratum",
  "start_marketing_date": "20230419",
  "active_numerator_strength": "1"
}

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