NDC 50730-8628 Antiseptic Hand Gel

NDC Product Code 50730-8628

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.

NDC Product Information

Antiseptic Hand Gel with NDC 50730-8628 is a product labeled by H And P Industries, Inc. Dba Triad Group. The generic name of Antiseptic Hand Gel 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.

  • 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)

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: 11-17-1997 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".

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Antiseptic Hand Gel Product Label Images

Antiseptic Hand Gel 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 Ingredient

Ethyl Alcohol, 70% v/v

Purpose

Antiseptic

Uses

  • For handwashing when water is not available to decrease bacteria on the skinafter changing diapersafter assisting ill personsbefore contact with a person under medical care or treatmentrecommended for repeated use

Warnings

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

Do Not Use

In the eyes.

Stop Use And Ask A Doctor

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

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 handSpread on both hands and rub into skin until dry (approx. 1-2 min.)Place a smaller amount into one handSpread over hands to wrist and rub into skin until dry (approx. 30 sec.)

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

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.