NDC 66096-749 Spongilla Lacustris Mt

Spongilla Lacustris

NDC Product Code 66096-749

NDC Product Information

Spongilla Lacustris Mt with NDC 66096-749 is a a human prescription drug product labeled by Ohm Pharma Inc.. The generic name of Spongilla Lacustris Mt is spongilla lacustris. The product's dosage form is tincture and is administered via oral form.

Labeler Name: Ohm Pharma Inc.

Dosage Form: Tincture - An alcoholic or hydroalcoholic solution prepared from vegetable materials or from chemical substances.

Product Type: Human Prescription Drug Additional informationCallout TooltipWhat kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.


Spongilla Lacustris Mt Active Ingredient(s)

Additional informationCallout TooltipWhat is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SPONGILLA LACUSTRIS 1 [hp_X]/.25L

Inactive Ingredient(s)

Additional informationCallout TooltipAbout the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

Additional informationCallout TooltipWhat are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

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Spongilla Lacustris Mt Product Label Images

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