NDC 57955-2551 Neglectful
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 57955-2551?
What are the uses for Neglectful?
Which are Neglectful UNII Codes?
The UNII codes for the active ingredients in this product are:
- BROMUS RAMOSUS FLOWER (UNII: 0W9O574LE8)
- BROMUS RAMOSUS FLOWER (UNII: 0W9O574LE8) (Active Moiety)
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
- CARPINUS BETULUS FLOWERING TOP (UNII: QOI241B01F)
- CARPINUS BETULUS FLOWERING TOP (UNII: QOI241B01F) (Active Moiety)
- CYTISUS SCOPARIUS FLOWERING TOP (UNII: XZC6H8R666)
- CYTISUS SCOPARIUS FLOWERING TOP (UNII: XZC6H8R666) (Active Moiety)
- GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ)
- GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ) (Active Moiety)
- HELLEBORUS NIGER ROOT (UNII: 608DGJ6815)
- HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (Active Moiety)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- MENTHA PIPERITA (UNII: 79M2M2UDA9) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4)
- SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4) (Active Moiety)
- SCLERANTHUS ANNUUS FLOWERING TOP (UNII: CC4B5WU2XX)
- SCLERANTHUS ANNUUS FLOWERING TOP (UNII: CC4B5WU2XX) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Neglectful 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:
- WATER (UNII: 059QF0KO0R)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".