NDC 68088-515 Landrum Instant Hand Sanitizer

NDC Product Code 68088-515

NDC 68088-515-62

Package Description: 237 mL in 1 BOTTLE

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

NDC Product Information

Landrum Instant Hand Sanitizer with NDC 68088-515 is a product labeled by Kentucky Technology Llc.. The generic name of Landrum Instant Hand Sanitizer is . The product's dosage form is and is administered via form.

Labeler Name: Kentucky Technology Llc.

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)
  • CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
  • ALOE (UNII: V5VD430YW9)
  • TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

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

Labeler Name: Kentucky Technology Llc.
Labeler Code: 68088
Start Marketing Date: 05-21-2010 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.

Landrum Instant Hand Sanitizer Product Label Images

Landrum Instant Hand Sanitizer 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

Other

Drug Facts

  • Other InformationStore in a cool dry place below 104° F.

Otc - Active Ingredient

Active Ingredient:Ethanol (60% v/v)

Otc - Purpose

Purpose:Anti-Microbial Hand Sanitizer

Indications & Usage

  • UsesHelps reduce bacteria that potentially can cause disease
  • Helps prevent cross contamination by hand contact
  • Recommended for repeated use

Warnings

  • WarningsFor external use onlyFlammable, keep away from fire, heat, or flameKeep out of reach of children.Do not use near eyes
  • In case of eye contact flush with water for 15 minutes
  • If irritation persists stop use of product and get medical attention
  • In case of accidental ingestion seek medical attention or contact a poison control center immediately.

Dosage & Administration

  • DirectionsUse no water or towels
  • Apply appropriate amount of product to palm of hand
  • Rub until hands are completely covered
  • Agitate lightly until dry
  • Let air dry for 15 seconds
  • Do not rinse or wipe with towel.

Inactive Ingredient

Inactive IngredientsWater, Carbomer, Triethanolamine, PEG-75 Lanolin, Aloe Vera Gel, Fragrance.

* Please review the disclaimer below.