NDC 61657-0052 Bactoflam

Echinacea, Baptisia, Apis Mellifica , Ferrum Phosphoricum ,

NDC Product Code 61657-0052

NDC 61657-0052-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bactoflam with NDC 61657-0052 is a a human over the counter drug product labeled by White Manufacturing Inc. Dba Micro West. The generic name of Bactoflam is echinacea, baptisia, apis mellifica , ferrum phosphoricum , . The product's dosage form is liquid and is administered via oral form.

Labeler Name: White Manufacturing Inc. Dba Micro West

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Bactoflam Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ECHINACEA, UNSPECIFIED 3 [hp_X]/30mL
  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/30mL
  • APIS MELLIFERA 12 [hp_X]/30mL
  • FERRUM PHOSPHORICUM 12 [hp_X]/30mL
  • ATROPA BELLADONNA 12 [hp_X]/30mL
  • TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/30mL
  • ARSENIC TRIOXIDE 12 [hp_X]/30mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: White Manufacturing Inc. Dba Micro West
Labeler Code: 61657
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 06-10-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Bactoflam Product Label Images

Bactoflam Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Apis mel 12XArsenicum alb 12XBaptisia 3XBelladonna 12XEchinacea 3XFerrum phos 12XRhus tox 12X

Inactive Ingredient

Alcohol (20% v/v, Purified water

Purpose

TEMPORARY RELIEF OF HEAT, REDNESS, SWELLING DUE TO INFLAMMATION

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Warnings

WARNINGS: STOP USE AND CALL A DOCTOR IF symptoms persist or worsen. IF PREGNANT OR BREAST FEEDING, consult a healthcare professional before use. CONTAINS ALCOHOL: in case of accidental overdose, consult a poison control center immediately

Indications

FOR THE TEMPORARY RELIEF OF HEAT, REDNESS, SWELLING DUE TO INFLAMMATION

Directions

Take 6 drops orally, 4 times a day. For ages 2 to adult.

Manufacture

MANUFACTURED FOR MICRO WESTDOUGLAS, WY 826331-307-358-5066

Other Information

Tamper resistant for you protection; use only if safety seal is intact

* Please review the disclaimer below.