NDC 71919-388

Kali silicatum

Potassium Silicate

Kali silicatum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Potassium Silicate.

Product ID71919-388_7e561858-cc3b-3334-e053-2991aa0af15c
NDC71919-388
Product TypeHuman Otc Drug
Proprietary NameKali silicatum
Generic NamePotassium Silicate
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2015-07-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NamePOTASSIUM SILICATE
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-388-07

15 mL in 1 VIAL, GLASS (71919-388-07)
Marketing Start Date2015-07-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-388-07 [71919038807]

Kali silicatum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-07-27

NDC 71919-388-08 [71919038808]

Kali silicatum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-07-27

NDC 71919-388-10 [71919038810]

Kali silicatum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-07-27

NDC 71919-388-09 [71919038809]

Kali silicatum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-07-27

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM SILICATE30 [hp_C]/mL

OpenFDA Data

SPL SET ID:0734c9a2-d999-4252-8739-120bd0112c64
Manufacturer
UNII
UPC Code
  • 0740640359242
  • NDC Crossover Matching brand name "Kali silicatum" or generic name "Potassium Silicate"

    NDCBrand NameGeneric Name
    68428-966Kali silicatumPOTASSIUM SILICATE
    71919-388Kali silicatumPOTASSIUM SILICATE
    64117-247RUNNY NOSEPOTASSIUM SILICATE

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