NDC 43742-1008 Gi Drainage

Gi Drainage with NDC 43742-1008 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Gi Drainage is cinnamomum, gentiana lutea, syzygium jambolanum, argentum nitricum, colchicum autumnale, colostrum, copper gluconate, lappa major, lycopodium clavatum, magnesium gluconate, manganese gluconate, nitricum acidum, pancreas suis, potassium gluconate, rumex crispus, schrophu8laria nodosa, stomach (suis), aurum metallicum, beech, calcarea carbonica, carbo vegetabilis, cherry plum, crab apple, intestine (suis), rock water, fagus sylvatica, flos. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What 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.

Gi Drainage Active Ingredient(s)

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

• CINNAMON 3 [hp_X]/mL
• GENTIANA LUTEA ROOT 3 [hp_X]/mL
• SYZYGIUM CUMINI SEED 3 [hp_X]/mL
• SILVER NITRATE 6 [hp_X]/mL
• COLCHICUM AUTUMNALE BULB 6 [hp_X]/mL
• BOS TAURUS COLOSTRUM 6 [hp_X]/mL
• COPPER GLUCONATE 6 [hp_X]/mL
• ARCTIUM LAPPA ROOT 6 [hp_X]/mL
• LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
• MAGNESIUM GLUCONATE 6 [hp_X]/mL
• MANGANESE GLUCONATE 6 [hp_X]/mL
• NITRIC ACID 6 [hp_X]/mL
• SUS SCROFA PANCREAS 6 [hp_X]/mL
• POTASSIUM GLUCONATE 6 [hp_X]/mL
• RUMEX CRISPUS ROOT 6 [hp_X]/mL
• SCROPHULARIA NODOSA 6 [hp_X]/mL
• SUS SCROFA STOMACH 6 [hp_X]/mL
• GOLD 8 [hp_X]/mL
• OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL
• ACTIVATED CHARCOAL 8 [hp_X]/mL
• PORK INTESTINE 8 [hp_X]/mL
• MALUS PUMILA FLOWER 8 [hp_X]/mL
• PRUNUS CERASIFERA FLOWER 8 [hp_X]/mL
• FAGUS SYLVATICA FLOWERING TOP 12 [hp_X]/mL

Inactive Ingredient(s)

About 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)

What 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

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date: 05-19-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
End Marketing Date: 07-19-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

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