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  4. NDC Product Code: 43772-0003 Bacsode

NDC 43772-0003 Bacsode

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43772-0003?
  4. Bacsode Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Get all the details for National Drug Code (NDC) 43772-0003 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
43772-0003
Proprietary Name:
Bacsode
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Synergy Formulas, Inc.
Labeler Code:
43772
Product Label ID:
ee7a0b88-81c5-493f-913f-5073f8b4a487
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
03-29-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 43772-0003?

The NDC code 43772-0003 is assigned by the FDA to the product Bacsode which is product labeled by Synergy Formulas, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43772-0003-1 60 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Bacsode?

Balances the antibacterial systems of the body. Balances the antibacterial systems of the body.

Which are Bacsode UNII Codes?

The UNII codes for the active ingredients in this product are:

  • GOLDENSEAL (UNII: ZW3Z11D0JV)
  • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
  • MYRRH (UNII: JC71GJ1F3L)
  • MYRRH (UNII: JC71GJ1F3L) (Active Moiety)
  • TABEBUIA IMPETIGINOSA BARK (UNII: 6GLA1946WX)
  • TABEBUIA IMPETIGINOSA BARK (UNII: 6GLA1946WX) (Active Moiety)
  • ATROPA BELLADONNA WHOLE (UNII: DSV74G1P2J)
  • ATROPA BELLADONNA WHOLE (UNII: DSV74G1P2J) (Active Moiety)
  • BOS TAURUS THYMUS (UNII: 8XEJ88V2T8)
  • BOS TAURUS THYMUS (UNII: 8XEJ88V2T8) (Active Moiety)
  • BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29)
  • BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (Active Moiety)
  • BOS TAURUS SPLEEN (UNII: 190Q9MB3U3)
  • BOS TAURUS SPLEEN (UNII: 190Q9MB3U3) (Active Moiety)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
  • PHOSPHORUS (UNII: 27YLU75U4W)
  • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
  • CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956)
  • CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (Active Moiety)
  • LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N)
  • LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N) (Active Moiety)
  • BOTULINUM TOXIN TYPE A (UNII: E211KPY694)
  • ABOBOTULINUMTOXINA (UNII: E211KPY694) (Active Moiety)
  • CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44)
  • CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44) (Active Moiety)
  • CLOSTRIDIUM TETANI (UNII: 751E8J54VM)
  • CLOSTRIDIUM TETANI (UNII: 751E8J54VM) (Active Moiety)
  • ESCHERICHIA COLI (UNII: 514B9K0L10)
  • ESCHERICHIA COLI (UNII: 514B9K0L10) (Active Moiety)
  • NEISSERIA MENINGITIDIS (UNII: V3TP2MD7F3)
  • NEISSERIA MENINGITIDIS (UNII: V3TP2MD7F3) (Active Moiety)
  • PASTEURELLA MULTOCIDA (UNII: IX56B2GQX6)
  • PASTEURELLA MULTOCIDA (UNII: IX56B2GQX6) (Active Moiety)
  • STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2)
  • STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2) (Active Moiety)
  • PROTEUS VULGARIS (UNII: 11T9HCO30O)
  • PROTEUS VULGARIS (UNII: 11T9HCO30O) (Active Moiety)
  • PSEUDOMONAS AERUGINOSA (UNII: Y793W5V55N)
  • PSEUDOMONAS AERUGINOSA (UNII: Y793W5V55N) (Active Moiety)
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (Active Moiety)
  • STAPHYLOCOCCUS AUREUS (UNII: O478WX4004)
  • STAPHYLOCOCCUS AUREUS (UNII: O478WX4004) (Active Moiety)
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O)
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O) (Active Moiety)

Which are Bacsode 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:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".