NDC 50730-8628 Antiseptic Hand Gel

Product Information

Product Code50730-8628
Proprietary Name 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.
Antiseptic Hand Gel
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
H And P Industries, Inc. Dba Triad Group
Labeler Code50730
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
11-17-1997
Listing Expiration Date 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.
12-31-2017
Exclude Flag 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".
I
NDC Code Structure

Usage Information


Product Packages

NDC 50730-8628-7

Package Description: 3.79 L in 1 BOTTLE, PLASTIC

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

Product Details

Antiseptic Hand Gel is product labeled by H And P Industries, Inc. Dba Triad Group. The product's dosage form is and is administered via form.


What are Antiseptic Hand Gel Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL (UNII: 3K9958V90M)
  • ALCOHOL (UNII: 3K9958V90M) (Active Moiety)


NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:


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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
  • DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
  • POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4)
  • TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • WATER (UNII: 059QF0KO0R)


* Please review the disclaimer below.

Antiseptic Hand Gel Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Active Ingredient



Ethyl Alcohol, 70% v/v


Purpose



Antiseptic


Uses



For handwashing when water is not available to decrease bacteria on the skin

  • after changing diapers
  • after assisting ill persons
  • before contact with a person under medical care or treatment
  • recommended for repeated use

Warnings



For external use only.Flammable, keep away from fire or flame.



Do Not Use



In the eyes.

Otc - Ask Doctor/Pharmacist





Otc - When Using





Stop Use And Ask A Doctor



  • if irritation and redness develop.
  • if condition persists for more than 72 hours

Otc - Pregnancy Or Breast Feeding





Keep Out Of Reach Of Children



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


Directions



  • Place a palmful of product in one hand
  • Spread on both hands and rub into skin until dry (approx. 1-2 min.)
  • Place a smaller amount into one hand
  • Spread over hands to wrist and rub into skin until dry (approx. 30 sec.)

Other





Other Information



Store at room temperature: 15°- 30° C (59° - 86° F)

Inactive Ingredients



Aloe vera gel, carbomer 940, denatonium benzoate, fragrance, PEG-1450, tert-butyl alcohol, triethanolamine, water

Otc - Questions





Label Information



Triad®Cat. No. 10-8628NDC 50730-8628-7Antiseptic Hand GelReduces the risk of bacterial contamination and infectionHelps meet CDC, OSHA and APIC Guidelines for Hand HygieneContains Aloe Vera GelTriad Group, Inc.700 West North Shore DriveHartland, WI 53029MADE IN USAwww.triad-group.net128 fl. oz. (3.79L)

* Please review the disclaimer below.