NDC 57955-3021 Alcoholism
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-3021 - Alcoholism
Product Packages
NDC Code 57955-3021-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-3021?
What are the uses for Alcoholism?
Which are Alcoholism UNII Codes?
The UNII codes for the active ingredients in this product are:
- AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M)
- AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M) (Active Moiety)
- AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
- AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
- APOCYNUM CANNABINUM ROOT (UNII: 2F92409L9Z)
- APOCYNUM CANNABINUM ROOT (UNII: 2F92409L9Z) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- ASARUM EUROPAEUM (UNII: H0876AL67A)
- ASARUM EUROPAEUM (UNII: H0876AL67A) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
- CARBON DISULFIDE (UNII: S54S8B99E8)
- CARBON DISULFIDE (UNII: S54S8B99E8) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) (Active Moiety)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
- LONICERA CAPRIFOLIUM FLOWERING TOP (UNII: 1X0T378SXY)
- LONICERA CAPRIFOLIUM FLOWERING TOP (UNII: 1X0T378SXY) (Active Moiety)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
- PAULLINIA CUPANA SEED (UNII: C21GE7524R)
- PAULLINIA CUPANA SEED (UNII: C21GE7524R) (Active Moiety)
Which are Alcoholism 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)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- 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".