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  4. NDC Product Code: 63083-2148 Fibrous Breast Drops 2148

NDC 63083-2148 Fibrous Breast Drops 2148

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63083-2148?
  4. Fibrous Breast Drops 2148 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.
NDC Product Code:
63083-2148
Proprietary Name:
Fibrous Breast Drops 2148
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Professional Complementary Health Formulas
Labeler Code:
63083
Product Label ID:
373252f3-bbf5-48f1-b2d0-e089c793b18a
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 63083-2148?

The NDC code 63083-2148 is assigned by the FDA to the product Fibrous Breast Drops 2148 which is product labeled by Professional Complementary Health Formulas. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63083-2148-2 59 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 Fibrous Breast Drops 2148?

For the temporary relief of swollen, tender, sore, or painful breasts.*

Which are Fibrous Breast Drops 2148 UNII Codes?

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

  • ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8) (Active Moiety)
  • ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW)
  • ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW) (Active Moiety)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV)
  • BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV) (Active Moiety)
  • SUS SCROFA MAMMARY GLAND (UNII: 692OX2DX0E)
  • SUS SCROFA MAMMARY GLAND (UNII: 692OX2DX0E) (Active Moiety)
  • HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3)
  • HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3) (Active Moiety)
  • ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
  • ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
  • AETHUSA CYNAPIUM WHOLE (UNII: M6936L953C)
  • AETHUSA CYNAPIUM WHOLE (UNII: M6936L953C) (Active Moiety)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
  • ONOSMODIUM VIRGINIANUM (UNII: 604NK4250S)
  • ONOSMODIUM VIRGINIANUM (UNII: 604NK4250S) (Active Moiety)
  • SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4)
  • SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4) (Active Moiety)

Which are Fibrous Breast Drops 2148 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.

[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".