Hemorrhoids Relief

Horse Chestnut,aloe,hamamelis Virginiana Root Bark/stem Bark,nitric Acid,paeonia Officinalis Root,sepia Officinalis Juice.

Homeocare Laboratories
Human Otc Drug
NDC 61727-306

Hemorrhoids Relief also known as Horse Chestnut,aloe,hamamelis Virginiana Root Bark/stem Bark,nitric Acid,paeonia Officinalis Root,sepia Officinalis Juice. is a human otc drug labeled by 'Homeocare Laboratories'. National Drug Code (NDC) number for Hemorrhoids Relief is 61727-306. This drug is available in dosage form of Pellet. The names of the active, medicinal ingredients in Hemorrhoids Relief drug includes Aloe - 8 [hp_X]/4g Hamamelis Virginiana Root Bark/stem Bark - 8 [hp_X]/4g Horse Chestnut - 8 [hp_X]/4g Nitric Acid - 8 [hp_X]/4g Paeonia Officinalis Root - 8 [hp_X]/4g Sepia Officinalis Juice - 8 [hp_X]/4g . The currest status of Hemorrhoids Relief drug is Active.

Drug Information:

Drug NDC:	61727-306
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:	Hemorrhoids Relief
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:	Horse Chestnut,aloe,hamamelis Virginiana Root Bark/stem Bark,nitric Acid,paeonia Officinalis Root,sepia Officinalis Juice.
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Homeocare Laboratories
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Pellet
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:	ALOE - 8 [hp_X]/4g HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - 8 [hp_X]/4g HORSE CHESTNUT - 8 [hp_X]/4g NITRIC ACID - 8 [hp_X]/4g PAEONIA OFFICINALIS ROOT - 8 [hp_X]/4g SEPIA OFFICINALIS JUICE - 8 [hp_X]/4g
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	SUBLINGUAL
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:	20 Jul, 2012
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	10 Jun, 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:	Homeocare Laboratories
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.
UPC:	0361727306210
UPC stands for Universal Product Code.
UNII:	V5VD430YW9 T7S323PKJS 3C18L6RJAZ 411VRN1TV4 8R564U2E1P QDL83WN8C2
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.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
61727-306-21	4 g in 1 TUBE (61727-306-21)	20 Jul, 2012	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

Hemorrhoids Relief

Horse Chestnut & more..

Pellet
Homeocare Laboratories
NDC: 61727-306

Purpose:

Purpose: relieves pain and discomfort, soothes and reduces inflammation, burning, itching and swelling. improves venous circulation.

Product Elements:

Hemorrhoids relief horse chestnut,aloe,hamamelis virginiana root bark/stem bark,nitric acid,paeonia officinalis root,sepia officinalis juice. sucrose lactose horse chestnut horse chestnut aloe aloe hamamelis virginiana root bark/stem bark hamamelis virginiana root bark/stem bark nitric acid nitric acid paeonia officinalis root paeonia officinalis root sepia officinalis juice sepia officinalis juice

Indications and Usage:

Indications & usage: turn tube upside down, twist cap to break seal & release pellets. using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. take apart from food or drinks. to preserve purity avoid touching pellets with fingers.

Warnings:

Warnings: if symptoms persist or worsen, or if pregnant or nursing, consult a doctor. keep out of reach of children. do not use if cap seal is broken or missing.

Dosage and Administration:

Dosage & administration: turn tube upside down, twist cap to break seal & release pellets. using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. take apart from food or drinks.to preserve purity avoid touching pellets with fingers.

Package Label Principal Display Panel:

Hemorrhoids relief hemorrhoids relief homeopathic medicine 85 pellets hcl_label_hhoids 2012.jpg hemorrhoids relief image 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.