NDC 57520-0349 Colosode
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0349 - Colosode
Product Packages
NDC Code 57520-0349-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57520-0349?
What are the uses for Colosode?
Which are Colosode UNII Codes?
The UNII codes for the active ingredients in this product are:
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- FRANGULA PURSHIANA BARK (UNII: 4VBP01X99F)
- FRANGULA PURSHIANA BARK (UNII: 4VBP01X99F) (Active Moiety)
- RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M)
- RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M) (Active Moiety)
- ARTEMISIA CINA FLOWER (UNII: 28M1820ACT)
- ARTEMISIA CINA FLOWER (UNII: 28M1820ACT) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO) (Active Moiety)
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- SUS SCROFA GALLBLADDER (UNII: B6A98VOI9I)
- SUS SCROFA GALLBLADDER (UNII: B6A98VOI9I) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- PORK INTESTINE (UNII: 40GMI0R60L)
- PORK INTESTINE (UNII: 40GMI0R60L) (Active Moiety)
- ESCHERICHIA COLI (UNII: 514B9K0L10)
- ESCHERICHIA COLI (UNII: 514B9K0L10) (Active Moiety)
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5)
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5) (Active Moiety)
- CARBO ANIMALIS (UNII: 279O8I0433)
- CARBO ANIMALIS (UNII: 279O8I0433) (Active Moiety)
- ENTEROCOCCUS FAECALIS (UNII: 15E04LZ9CT)
- ENTEROCOCCUS FAECALIS (UNII: 15E04LZ9CT) (Active Moiety)
- MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB)
- MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- SELENIUM (UNII: H6241UJ22B)
- SELENIUM (UNII: H6241UJ22B) (Active Moiety)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (Active Moiety)
- PROTEUS MIRABILIS (UNII: C177VR41DV)
- PROTEUS MIRABILIS (UNII: C177VR41DV) (Active Moiety)
- PSEUDOMONAS AERUGINOSA (UNII: Y793W5V55N)
- PSEUDOMONAS AERUGINOSA (UNII: Y793W5V55N) (Active Moiety)
- INDOLE (UNII: 8724FJW4M5)
- INDOLE (UNII: 8724FJW4M5) (Active Moiety)
- CLOSTRIDIUM PERFRINGENS (UNII: OVP6XX033E)
- CLOSTRIDIUM PERFRINGENS (UNII: OVP6XX033E) (Active Moiety)
- BOTULINUM TOXIN TYPE A (UNII: E211KPY694)
- BOTULINUM TOXIN TYPE A (UNII: E211KPY694) (Active Moiety)
- GIARDIA LAMBLIA (UNII: 89IEJ09R73)
- GIARDIA LAMBLIA (UNII: 89IEJ09R73) (Active Moiety)
- YERSINIA ENTEROCOLITICA (UNII: AUL7Y5Z806)
- YERSINIA ENTEROCOLITICA (UNII: AUL7Y5Z806) (Active Moiety)
- COLOSTRUM HUMAN (UNII: VB6F65I6F5)
- COLOSTRUM HUMAN (UNII: VB6F65I6F5) (Active Moiety)
- SUS SCROFA GALLBLADDER (UNII: B6A98VOI9I)
- LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5)
- LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5) (Active Moiety)
Which are Colosode 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)
- 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".