NDC 43857-0464 Bio Biological Detox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43857 - Bioactive Nutritional, Inc.
- 43857-0464 - Bio Biological Detox
Product Packages
NDC Code 43857-0464-1
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 43857-0464?
What are the uses for Bio Biological Detox?
Which are Bio Biological Detox UNII Codes?
The UNII codes for the active ingredients in this product are:
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N)
- LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N) (Active Moiety)
- MYRRH (UNII: JC71GJ1F3L)
- MYRRH (UNII: JC71GJ1F3L) (Active Moiety)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF) (Active Moiety)
- TABEBUIA IMPETIGINOSA BARK (UNII: 6GLA1946WX)
- HANDROANTHUS IMPETIGINOSUS BARK (UNII: 6GLA1946WX) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- THYMUS SERPYLLUM (UNII: 86H4S6K51N)
- THYMUS SERPYLLUM (UNII: 86H4S6K51N) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L) (Active Moiety)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (Active Moiety)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- RANCID BEEF (UNII: 29SUH5R3HU)
- RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N)
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- CITHARACANTHUS SPINICRUS (UNII: 3Y5X6RT823)
- CITHARACANTHUS SPINICRUS (UNII: 3Y5X6RT823) (Active Moiety)
- VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK)
- VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK) (Active Moiety)
- BOTULINUM TOXIN TYPE A (UNII: E211KPY694)
- ABOBOTULINUMTOXINA (UNII: E211KPY694) (Active Moiety)
- SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J)
- SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J) (Active Moiety)
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (Active Moiety)
- FRANCISELLA TULARENSIS (UNII: NNR1301B0H)
- COXIELLA BURNETII (UNII: GRY5SDU86N) (Active Moiety)
- COXIELLA BURNETII (UNII: GRY5SDU86N)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT) (Active Moiety)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT)
- PLASMODIUM MALARIAE (UNII: AR76CST9I2)
- PLASMODIUM MALARIAE (UNII: AR76CST9I2) (Active Moiety)
- ESCHERICHIA COLI (UNII: 514B9K0L10)
- ESCHERICHIA COLI (UNII: 514B9K0L10) (Active Moiety)
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN)
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN) (Active Moiety)
- YERSINIA PESTIS (UNII: S6JJH3XV1D)
- YERSINIA PESTIS (UNII: S6JJH3XV1D) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Bio Biological Detox 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
* 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".