73421-0052 NDC - BACTOFLAM (APIS MEL, ARSENICUM ALB, BAPTISIA, BELLADONNA, ECHINACEA, FERRUM PHOS, RHUS TOX)

Drug Information

Product NDC: 73421-0052

Proprietary Name: BACTOFLAM

Non Proprietary Name: Apis mel, Arsenicum alb, Baptisia, Belladonna, Echinacea, Ferrum phos, Rhus tox

Active Ingredient(s):
  • 12 [hp_X]/29.6mL APIS MELLIFERA;
  • 12 [hp_X]/29.6mL ARSENIC TRIOXIDE;
  • 12 [hp_X]/29.6mL ATROPA BELLADONNA;
  • 3 [hp_X]/29.6mL BAPTISIA TINCTORIA ROOT;
  • 3 [hp_X]/29.6mL ECHINACEA, UNSPECIFIED;
  • 12 [hp_X]/29.6mL FERROSOFERRIC PHOSPHATE;
  • 12 [hp_X]/29.6mL TOXICODENDRON PUBESCENS LEAF


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Bee Venoms [CS];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Standardized Insect Venom Allergenic Extract [EPC]

Labeler Information

Labeler Name: White Manufacturing Inc. DBA Micro-West
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/1/2021

Package Information

No. Package Code Package Description Billing Unit
173421-0052-129.6 mL in 1 BOTTLE (73421-0052-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73421-0052The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEBACTOFLAMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEApis mel, Arsenicum alb, Baptisia, Belladonna, Echinacea, Ferrum phos, Rhus toxThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/1/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEWhite Manufacturing Inc. DBA Micro-WestName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAPIS MELLIFERA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BAPTISIA TINCTORIA ROOT; ECHINACEA, UNSPECIFIED; FERROSOFERRIC PHOSPHATE; TOXICODENDRON PUBESCENS LEAFAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 3; 3; 12; 12 
ACTIVE INGRED UNIT[hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL 
PHARM CLASSESAllergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC] 

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This page was last updated on: 2/1/2023