NDC 71389-101 Biotronix Healthcare

NDC Product Code 71389-101

NDC CODE: 71389-101

Proprietary Name: Biotronix Healthcare 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.

NDC Code Structure

  • 71389 - Biotronix Healthcare Industries, Inc.

NDC 71389-101-01

Package Description: 20 mL in 1 POUCH

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

NDC Product Information

Biotronix Healthcare with NDC 71389-101 is a product labeled by Biotronix Healthcare Industries, Inc.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 797730.

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.

  • WATER (UNII: 059QF0KO0R)
  • HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
  • NONOXYNOL-10 (UNII: K7O76887AP)

Product Labeler Information

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

Labeler Name: Biotronix Healthcare Industries, Inc.
Labeler Code: 71389
Start Marketing Date: 05-03-2018 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: 12-31-2019 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.

Biotronix Healthcare Product Label Images

Biotronix Healthcare 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

Otc - Active Ingredient

Active ingredientPovidone Iodine 10%

Otc - Purpose

Purpose
Antiseptic

Warnings

Warnings
For external use only. Do not use in the eyes.

Otc - Stop Use

Stop use and ask a doctor if Skin shows symptons of
irritation, sensitivity, redness, pain or swelling

Dosage & Administration

  • DirectionWet hands and forearms with waterClean under nails with nail cleanerScrub for 3 minutes with the impregnated brushPay close attention to the nails, cuticles, and interdigital spacesRinse thoroughly with running waterRepeat

Inactive Ingredient

Inactive ingredientsHydroxyethylcellulose, Nonoxynol ethoxylate, Purified Water

Indications & Usage

Uses For cleansing hands and arms prior to surgery

Other Safety Information

  • Other informationStore at room temperatureAvoid excessive heat above 40 °C (104 °F)Protect from freezingLatex free

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

* Please review the disclaimer below.