My Cycles Bff

Black Cohosh, Blue Cohosh, Calcium Carbonate, Chamomile, Graphites, High Cranberry, Poke Root, Potassium Carbonate, Potassium Hydrate, Sodium Chloride, Sulfur, Wind Flower

Knockout Remedy, Llc
Human Otc Drug
NDC 73274-001

My Cycles Bff also known as Black Cohosh, Blue Cohosh, Calcium Carbonate, Chamomile, Graphites, High Cranberry, Poke Root, Potassium Carbonate, Potassium Hydrate, Sodium Chloride, Sulfur, Wind Flower is a human otc drug labeled by 'Knockout Remedy, Llc'. National Drug Code (NDC) number for My Cycles Bff is 73274-001. This drug is available in dosage form of Tablet, Chewable. The names of the active, medicinal ingredients in My Cycles Bff drug includes Black Cohosh - 30 [hp_X]/1 Calcium Carbonate - 30 [hp_X]/1 Caulophyllum Thalictroides Root - 30 [hp_X]/1 Chamomile - 30 [hp_X]/1 Graphite - 30 [hp_X]/1 Phytolacca Americana Root - 30 [hp_X]/1 Potassium Carbonate - 30 [hp_X]/1 Potassium Hydroxide - 30 [hp_X]/1 Pulsatilla Vulgaris - 30 [hp_X]/1 Sodium Chloride - 30 [hp_X]/1 and more. The currest status of My Cycles Bff drug is Active.

Drug Information:

Drug NDC:	73274-001
The 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.
Proprietary Name:	My Cycles Bff
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Black Cohosh, Blue Cohosh, Calcium Carbonate, Chamomile, Graphites, High Cranberry, Poke Root, Potassium Carbonate, Potassium Hydrate, Sodium Chloride, Sulfur, Wind Flower
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Knockout Remedy, Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Tablet, Chewable
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	BLACK COHOSH - 30 [hp_X]/1 CALCIUM CARBONATE - 30 [hp_X]/1 CAULOPHYLLUM THALICTROIDES ROOT - 30 [hp_X]/1 CHAMOMILE - 30 [hp_X]/1 GRAPHITE - 30 [hp_X]/1 PHYTOLACCA AMERICANA ROOT - 30 [hp_X]/1 POTASSIUM CARBONATE - 30 [hp_X]/1 POTASSIUM HYDROXIDE - 30 [hp_X]/1 PULSATILLA VULGARIS - 30 [hp_X]/1 SODIUM CHLORIDE - 30 [hp_X]/1 Load more... SULFUR - 30 [hp_X]/1 VIBURNUM OPULUS ROOT - 30 [hp_X]/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	18 May, 2021
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	06 May, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Knockout Remedy, LLC
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UNII:	K73E24S6X9 H0G9379FGK JTJ6HH6YEH FGL3685T2X 4QQN74LH4O 11E6VI8VEG BQN1B9B9HA WZH3C48M4T I76KB35JEV 451W47IQ8X Load more... 70FD1KFU70 6N0G8XY3T8
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:	Blood Coagulation Factor [EPC] Calcium [CS] Cations Divalent [CS] Increased Coagulation Factor Activity [PE]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
73274-001-60	60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (73274-001-60)	18 May, 2021	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

My Cycles Bff

Black Cohosh & more..

Tablet, Chewable
Knockout Remedy, LLC
NDC: 73274-001

Purpose:

Purpose homeopathic pms relief

Product Elements:

My cycles bff black cohosh, blue cohosh, calcium carbonate, chamomile, graphites, high cranberry, poke root, potassium carbonate, potassium hydrate, sodium chloride, sulfur, wind flower viburnum opulus root viburnum opulus root caulophyllum thalictroides root caulophyllum thalictroides root pulsatilla vulgaris pulsatilla vulgaris phytolacca americana root phytolacca americana root potassium hydroxide hydroxide ion potassium carbonate carbonate ion sulfur sulfur black cohosh black cohosh sodium chloride chloride ion chamomile chamomile lactose monohydrate calcium carbonate calcium cation graphite graphite magnesium stearate

Indications and Usage:

Uses relieves [reduces the severity of] premenstrual syndrome (pms) symptoms: acne, backache, breast tenderness & swelling, cramping, fatigue, gastic symptoms, headache, mood changes, nausea

Warnings:

Warnings stop use and ask a doctor is symptoms persist or worsen. if pregnant or breast-feeding, ask a health professional before use.

Dosage and Administration:

Directions ages 12 years & up, take 1 tablet twice a day beginning around ovulation (ovulation usually occurs around day 14 of your cycle, with day 1 of your cycle being the first day of your period) through the first 3 days of your period. seperate doses by at least 10 hours.

Package Label Principal Display Panel:

Label my cycle bff label

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.