NDC 44911-0660 Organdrainex
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 44911-0660?
What are the uses for Organdrainex?
Which are Organdrainex UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- GARLIC (UNII: V1V998DC17)
- GARLIC (UNII: V1V998DC17) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR)
- COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (Active Moiety)
- CYNARA SCOLYMUS LEAF (UNII: B71UA545DE)
- CYNARA SCOLYMUS LEAF (UNII: B71UA545DE) (Active Moiety)
- PETROSELINUM CRISPUM WHOLE (UNII: 1WZA4Y92EX)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (Active Moiety)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W) (Active Moiety)
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
- PALLADIUM (UNII: 5TWQ1V240M)
- PALLADIUM (UNII: 5TWQ1V240M) (Active Moiety)
Which are Organdrainex Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".