NDC 57955-2300 Complaining
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 57955-2300?
What are the uses for Complaining?
Which are Complaining UNII Codes?
The UNII codes for the active ingredients in this product are:
- DILL (UNII: Y05PC4JZRH)
- DILL (UNII: Y05PC4JZRH) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- ASAFETIDA (UNII: W9FZA51AS1)
- ASAFETIDA (UNII: W9FZA51AS1) (Active Moiety)
- MAHONIA AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB)
- MAHONIA AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB) (Active Moiety)
- BISMUTH (UNII: U015TT5I8H)
- BISMUTH (UNII: U015TT5I8H) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U)
- FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U) (Active Moiety)
- ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W)
- ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R)
- SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
Which are Complaining 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".