NDC 64709-150 La Fresh Hand Sanitizing Wipe

Kills 99.9% Of Germs

NDC Product Code 64709-150

NDC 64709-150-10

Package Description: 1 g in 1 PACKET

NDC Product Information

La Fresh Hand Sanitizing Wipe with NDC 64709-150 is a a human over the counter drug product labeled by Diamond Wipes International, Inc. The generic name of La Fresh Hand Sanitizing Wipe is kills 99.9% of germs. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Diamond Wipes International, 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.

La Fresh Hand Sanitizing Wipe 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.

  • ALCOHOL 65 g/100g

Administration Route(s)

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

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Diamond Wipes International, Inc
Labeler Code: 64709
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: 11-02-2020 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’.

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La Fresh Hand Sanitizing Wipe Product Label Images

La Fresh Hand Sanitizing Wipe 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

Aluminum Chlorohydrate 15%




Reduce underarm perspiration


For external use onlyDo not use on broken skin
Stop use if rash or irritation occurs
Ask a doctor before use if you have kidney disease

Keep Out Of Reach Of Children

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


  • Open packetremove and unfold wipeapply to underarm only

Inactive Ingredients

Benzyl Alcohol, Fragrance, PEG-180, Phenoxyethanol, Polysorbate 20, Potassium Sorbate, Salvia Officinalis (Sage) Leaf Extract, Tocopherol, Tocopheryl Acetate, Usnea Barbata (Lichen) Extract, Water


LA FRESHtravel liteAntiperspirant Wipepowerful wetness & odor protectioninvisible, non-whitening formulafreshly scented1 wipe 5.75" x 1.75" (14.6cm x 19.6 cm)FSC FSC C109834 MIX PaperRAINFOREST ALLIANCE CERTIFIEDFor a refreshing getaway any day, Travel Lite and Live.Life.La FreshLike us on Facebook. Follow us on Twitter and Instagram. Pin with us on Pinterest.Made in USA of foreign and domestic componentsDistributed by La Fresh Group, IncChino, CA 91710www.LaFreshGroup.com2015 La Fresh Group, Inc.Item#F5324P PL-5324UPC 766670053240

* Please review the disclaimer below.