NDC 63824-450 Lysol No Touch

NDC Product Code 63824-450

NDC 63824-450-01

Package Description: 1 BOTTLE in 1 BLISTER PACK > 251 mL in 1 BOTTLE

NDC 63824-450-02

Package Description: 2 BOTTLE in 1 CARTON > 251 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

Lysol No Touch with NDC 63824-450 is a product labeled by Reckitt Benckiser Llc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 1039026 and 1039030.

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
  • LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)
  • PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
  • LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • SULISOBENZONE (UNII: 1W6L629B4K)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Labeler Information

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

Labeler Name: Reckitt Benckiser Llc
Labeler Code: 63824
Start Marketing Date: 09-15-2011 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: 12-31-2018 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.

Lysol No Touch 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

Distributed by: Reckitt Benckiser LLCParsippany, NJ 07054-0224

Active Ingredient

Benzethonium chloride, 0.13%

Purpose

Antibacterial

Use

For handwashing to decrease bacteria on the skin

Warnings

For external use only

When Using This Product

  • Avoid contact with eyes.In case of eye contact, flush with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develops.

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.

Directions

  • Wet hands.Place hands under dispenser until soap is dispensed.Wash hands.Rinse hands with water.Dry hands after rinsing.

Other Information

Store at room temperature

Inactive Ingredients

Water, Glycerin, Cetrimonium Chloride, Lauramide DEA, PEG-150 Distearate, Lauramine Oxide, Fragrance, Citric Acid, Tetrasodium EDTA, Benzophenone-4, Acrylates/PEG-10 Maleate/Styrene Copolymer, Di-PPG-2 Myreth-10 Adipate, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Yellow 5, D&C Orange 4, D&C Red 33 and FD&C Blue 1.

* Please review the disclaimer below.