Argentum Iodatum

UNIISPLATC D08AL30

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC codeD08AL30

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766227221
200 PELLET in 1 VIAL, GLASS (37662-2722-1)
ndc11
3766227222
500 PELLET in 1 VIAL, GLASS (37662-2722-2)
ndc11
3766227223
3000 PELLET in 1 BOTTLE, GLASS (37662-2722-3)
ndc11
3766227224
10000 PELLET in 1 BOTTLE, GLASS (37662-2722-4)

Annotations

UNII (FDA Substance ID)

81M6Z3D1XE

SILVER IODIDE

RxCUI 1423914

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "81M6Z3D1XE",
    "rxcui": "1423914",
    "inchikey": "MSFPLIAKTHOCQP-UHFFFAOYSA-M",
    "display_name": "SILVER IODIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4bd30e47-c039-06e8-e063-6294a90a8c4d": {
      "match": "brand_token",
      "title": "ARGENTUM 5X OINTMENT [URIEL PHARMACY, INC]",
      "spl_version": "1",
      "published_date": "2026-03-02"
    }
  },
  "productid": "37662-2722_f57bac38-bbd1-74f3-e053-2a95a90a6761",
  "productndc": "37662-2722",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SILVER IODIDE",
  "proprietary_name": "Argentum Iodatum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Argentum Iodatum",
  "start_marketing_date": "20230224",
  "active_numerator_strength": "200"
}

Related drugs

Other records sharing ATC code D08AL30.

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