Breast Care Liquid
NDC Package 55714-2394-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Breast Care (bufo rana, apis mel., asterias rubens, belladonna, bryonia, calc. carb., chamomilla, chimaphila umbellata, cinchona, conium, croton, echinacea, graphites, helonias dioica, lachesis, merc. viv., phellandrium aquaticum phosphorus, phytolacca, pulsatilla, sanguinaria, silicea, hamamelis, ruta, taraxacum) liquids is formulated for associated symptoms such as breast tenderness, nursing discomfort and pre-menstrual swelling. This formulation utilizes a liquid delivery system. Marketed by Newton Laboratories, Inc., this product is identified by NDC 55714-2394.

Identification & Billing

NDC Package Code
55714-2394-2
Package Description
50 mL in 1 BOTTLE, GLASS
Product Code
55714-2394
11-Digit Billing Format
55714239402

Clinical Specifications

Proprietary Name
Breast Care
Non-Proprietary Name
Bufo Rana, Apis Mel., Asterias Rubens, Belladonna, Bryonia, Calc. Carb., Chamomilla, Chimaphila Umbellata, Cinchona, Conium, Croton, Echinacea, Graphites, Helonias Dioica, Lachesis, Merc. Viv., Phellandrium Aquaticum Phosphorus, Phytolacca, Pulsatilla, Sanguinaria, Silicea, Hamamelis, Ruta, Taraxacum
Substance Name
Apis Mellifera; Asterias Rubens; Atropa Belladonna; Bryonia Alba Root; Bufo Bufo Cutaneous Gland; Chamaelirium Luteum Root; Chimaphila Umbellata; Cinchona Officinalis Bark; Conium Maculatum Flowering Top; Croton Tiglium Seed; Echinacea, Unspecified; Graphite; Hamamelis Virginiana Root Bark/stem Bark; Lachesis Muta Venom; Matricaria Recutita; Mercury; Oenanthe Aquatica Fruit; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Phytolacca Americana Root; Pulsatilla Vulgaris; Ruta Graveolens Flowering Top; Sanguinaria Canadensis Root; Silicon Dioxide; Taraxacum Officinale
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.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Formulated for associated symptoms such as breast tenderness, nursing discomfort and pre-menstrual swelling.

Regulatory & Marketing

Labeler Name
Newton Laboratories, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
11-05-2018
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (55714-2394). Click a package code to view its specific billing and regulatory data.

55714-2394-0
15 mL in 1 BOTTLE, GLASS
55714-2394-1
30 mL in 1 BOTTLE, GLASS

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 55714-2394-2 identifies a specific commercial package of 50 ml in 1 bottle, glass of Breast Care, a human over the counter drug labeled by Newton Laboratories, Inc.. This liquid is formulated for oral use and contains apis mellifera; asterias rubens; atropa belladonna; bryonia alba root; bufo bufo cutaneous gland; chamaelirium luteum root; chimaphila umbellata; cinchona officinalis bark; conium maculatum flowering top; croton tiglium seed; echinacea, unspecified; graphite; hamamelis virginiana root bark/stem bark; lachesis muta venom; matricaria recutita; mercury; oenanthe aquatica fruit; oyster shell calcium carbonate, crude; phosphorus; phytolacca americana root; pulsatilla vulgaris; ruta graveolens flowering top; sanguinaria canadensis root; silicon dioxide; taraxacum officinale as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Newton Laboratories, Inc. on November 05, 2018. The current certification is valid through December 31, 2026.

How is this Newton Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55714239402. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
55714-2394-2
11-Digit CMS (5-4-2)
55714-2394-02

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.