NDC 57955-1221 Common Cold
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc
- 57955-1221 - Common Cold
Product Packages
NDC Code 57955-1221-1
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 30 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 57955-1221?
What are the uses for Common Cold?
Which are Common Cold UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- SILVER IODIDE (UNII: 81M6Z3D1XE)
- SILVER IODIDE (UNII: 81M6Z3D1XE) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- SILVER CHLORIDE (UNII: MWB0804EO7)
- SILVER OXIDE (UNII: 897WUN6G6T)
- SILVER OXIDE (UNII: 897WUN6G6T) (Active Moiety)
- SILVER PHOSPHATE (UNII: ZL6T4Y1XP8)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- ANEMONE PULSATILLA (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- DRIMIA MARITIMA BULB (UNII: 3629601H5D)
- DRIMIA MARITIMA BULB (UNII: 3629601H5D) (Active Moiety)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (Active Moiety)
Which are Common Cold 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- WATER (UNII: 059QF0KO0R)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- STEVIOL (UNII: 4741LYX6RT)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GINGER OIL (UNII: SAS9Z1SVUK)
* 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".