NDC 57520-0219 Amoebasode
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0219 - Amoebasode
Product Packages
NDC Code 57520-0219-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57520-0219?
What are the uses for Amoebasode?
Which are Amoebasode UNII Codes?
The UNII codes for the active ingredients in this product are:
- WHEAT (UNII: 4J2I0SN84Y)
- WHEAT (UNII: 4J2I0SN84Y) (Active Moiety)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
- JATEORHIZA CALUMBA ROOT (UNII: V36I2B8LD5)
- JATEORHIZA CALUMBA ROOT (UNII: V36I2B8LD5) (Active Moiety)
- FRAGARIA VESCA FRUIT (UNII: CG6IX3GCMU)
- FRAGARIA VESCA FRUIT (UNII: CG6IX3GCMU) (Active Moiety)
- QUASSIA AMARA WOOD (UNII: S5249Q85HW)
- QUASSIA AMARA WOOD (UNII: S5249Q85HW) (Active Moiety)
- SENNA LEAF (UNII: AK7JF626KX)
- SENNA LEAF (UNII: AK7JF626KX) (Active Moiety)
- WORMWOOD (UNII: F84709P2XV)
- WORMWOOD (UNII: F84709P2XV) (Active Moiety)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (Active Moiety)
- CAJUPUT OIL (UNII: J3TO6BUQ37)
- CAJUPUT OIL (UNII: J3TO6BUQ37) (Active Moiety)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (Active Moiety)
- AMOEBA PROTEUS (UNII: APR291GFYV)
- AMOEBA PROTEUS (UNII: APR291GFYV) (Active Moiety)
- GIARDIA LAMBLIA (UNII: 89IEJ09R73)
- GIARDIA LAMBLIA (UNII: 89IEJ09R73) (Active Moiety)
Which are Amoebasode 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".