NDC 50730-4812 Phenylephrine Hydrochloride

  1. Labeler Index
  2. H And P Industries, Inc. Dba Triad Group
  3. NDC: 50730-4812 Phenylephrine Hydrochloride

NDC Product Code 50730-4812

NDC CODE: 50730-4812

Proprietary Name: Phenylephrine Hydrochloride What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 50730 - H And P Industries, Inc. Dba Triad Group

NDC 50730-4812-0

Package Description: 12 SUPPOSITORY in 1 BOX

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Phenylephrine Hydrochloride with NDC 50730-4812 is a product labeled by H And P Industries, Inc. Dba Triad Group. The generic name of Phenylephrine Hydrochloride is . The product's dosage form is and is administered via form.

Labeler Name: H And P Industries, Inc. Dba Triad Group

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.
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • STARCH, CORN (UNII: O8232NY3SJ)

Product Labeler Information

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

Labeler Name: H And P Industries, Inc. Dba Triad Group
Labeler Code: 50730
Start Marketing Date: 03-01-2009 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Phenylephrine Hydrochloride Product Label Images

Phenylephrine Hydrochloride 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

Cocoa butter, 85.5%Phenylephrine HCI, 0.25%Shark liver oil, 3.0%

Purpose

Protectantvasoconstrictorprotectant

Uses

  • Temporarily shrinks hemorrhoidal tissuetemporarily relieves itching burning and discomfort associated with hemorrhoids

Warnings

For rectal use only.

Ask A Doctor Before Use If You Have

  • Heart diseasethyroid diseasedifficulty in urination due to enlargement of the prostate glandhigh blood pressurediabetes

Ask A Doctor Or Pharmacist Before Use If

You are presently taking a prescription drug for high blood pressure or depression.

When Using This Product

Do not exceed the recommended daily dosage.

Stop Use And Ask A Doctor If

  • You experience bleedingcondition worsens or does not improve within 7 days.These may be signs of a serious condition.

If Pregnant Or Breastfeeding

Ask a health professional before use.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults:When practical, cleanse the affected area by patting or blotting with an appropriate cleansing tissue. Gently dry by patting or blotting with toilet tissue or soft cloth before insertion of this product.Detach one suppository from stripRemove wrapper before inserting into rectumHold suppository with rounded end up and insert tip of fingernail at end marked "peel down"Carefully peel film slowly and evenly down both sides to expose suppositoryInsert one suppository into rectum up to 4 times daily especially at night and morning or after each bowel movementChildren under 12 years:  ask a doctor

Storage

Store in a cool place or at room temperature but not over 86° F.

Inactive Ingredients

Methylparaben, propylparaben, starch

Package Information

  • NDC 50730-4812-0Live BetterHemorrhoidal SuppositoriesPHENYLEPHRINE HCL 0.25%Temporary relief of burning, itching and discomfortProvides nighttime reliefShrinks swelling of irritated hemorrhoidal tissueProtects irritated tissueEasy to open12 SuppositoriesDISTRIBUTED BY OMNIPOINT, INC.2 PARAGON DRIVE, MONTVALE, NJ 076542009 ALL RIGHTS RESERVEDLive Better products provide a simple way to look after yourself and your family. All of our products are crafted from high quality ingredients to exacting standards.Live Better is a great way to meet the health needs of your busylifestyle. Live Better helps you be better.Live Better, for life.FOR YOUR SAFETY, SUPPOSITORIES ARE PACKAGED IN TAMPER-EVIDENT SEALED PLASTIC WRAPPER. DO NOT USE IF PLASTIC WRAPPER IS TORN OR OPEN.

* Please review the disclaimer below.