NDC 71919-100

Aurum iodatum

Gold Monoiodide

Aurum iodatum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Gold Monoiodide.

Product ID71919-100_7e395392-849f-6c6c-e053-2a91aa0af863
NDC71919-100
Product TypeHuman Otc Drug
Proprietary NameAurum iodatum
Generic NameGold Monoiodide
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2010-04-29
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameGOLD MONOIODIDE
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-100-07

15 mL in 1 VIAL, GLASS (71919-100-07)
Marketing Start Date2010-04-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-100-10 [71919010010]

Aurum iodatum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-29

NDC 71919-100-08 [71919010008]

Aurum iodatum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-29

NDC 71919-100-07 [71919010007]

Aurum iodatum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-29

NDC 71919-100-09 [71919010009]

Aurum iodatum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-29

Drug Details

Active Ingredients

IngredientStrength
GOLD MONOIODIDE30 [hp_C]/mL

OpenFDA Data

SPL SET ID:0c752972-e784-46f1-a389-1cee30ebba8b
Manufacturer
UNII
UPC Code
  • 0740640242902
  • NDC Crossover Matching brand name "Aurum iodatum" or generic name "Gold Monoiodide"

    NDCBrand NameGeneric Name
    0220-0630Aurum iodatumGOLD MONOIODIDE
    0220-0632Aurum iodatumGOLD MONOIODIDE
    15631-0064AURUM IODATUMAURUM IODATUM
    68428-239Aurum iodatumGOLD MONOIODIDE
    71919-100Aurum iodatumGOLD MONOIODIDE

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