NDC 70924-003 Touchpoint Hand Sanitizing Wipes Fragrance Free

Benzalkonium Chloride

NDC Product Code 70924-003

NDC 70924-003-01

Package Description: 320 CLOTH in 1 CANISTER

NDC 70924-003-02

Package Description: 500 CLOTH in 1 BAG

NDC 70924-003-03

Package Description: 1500 CLOTH in 1 BAG

NDC 70924-003-04

Package Description: 320 CLOTH in 1 POUCH

NDC Product Information

Touchpoint Hand Sanitizing Wipes Fragrance Free with NDC 70924-003 is a a human over the counter drug product labeled by Innocore Sales & Marketing Inc. The generic name of Touchpoint Hand Sanitizing Wipes Fragrance Free is benzalkonium chloride. The product's dosage form is cloth and is administered via cutaneous form.

Labeler Name: Innocore Sales & Marketing Inc

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Touchpoint Hand Sanitizing Wipes Fragrance Free Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BENZALKONIUM CHLORIDE 1.3 mg/1

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.

  • BENZOIC ACID (UNII: 8SKN0B0MIM)
  • CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
  • DEHYDROACETIC ACID (UNII: 2KAG279R6R)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Cutaneous - Administration to the skin.
  • Cutaneous - Administration to the skin.

Product Labeler Information

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

Labeler Name: Innocore Sales & Marketing Inc
Labeler Code: 70924
FDA Application Number: part333E What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-24-2020 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: 12-31-2021 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Touchpoint Hand Sanitizing Wipes Fragrance Free Product Label Images

Touchpoint Hand Sanitizing Wipes Fragrance Free 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

Active Ingredient

Benzalkonium Chloride 0.13

Purpose

Antimicrobal

Use

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

Warnings

For external use only.

Otc - When Using

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly in water.

Otc - Do Not Use

Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a physician.If swallowed get medical help or contact a poison control center immediately.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

  • Wet hands thoroughly with product and allow to dry.Be sure to use entire wipe.Discard after single use.Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

Benzoic Acid, Caprylyl/Capryl Oligoglucoside, Dehydroacetic Acid, Phenoxyethanol, Poly(Laurylglucoside)-7, Propylene Glycol, Water

Questions?

1.877.910.4809

* Please review the disclaimer below.