NDC 73315-0717 Hand Sanitizing Wipes

Ethyl Alcohol

NDC Product Code 73315-0717

NDC 73315-0717-4

Package Description: 1 mL in 1 POUCH

NDC Product Information

Hand Sanitizing Wipes with NDC 73315-0717 is a a human over the counter drug product labeled by Grove Collaborative. The generic name of Hand Sanitizing Wipes is ethyl alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Grove Collaborative

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.

Hand Sanitizing Wipes 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 mL/100mL

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.

  • OAT (UNII: Z6J799EAJK)
  • 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.

  • 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: Grove Collaborative
Labeler Code: 73315
FDA Application Number: part333A 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: 04-01-2021 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 - NO 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.

Hand Sanitizing Wipes Product Label Images

Hand Sanitizing Wipes 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(S)

Ethyl Alcohol 65% v/v. Purpose: Antimicrobial




Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when water and soap are not available. Recommended for repeated use.Store in a cool, dry place away from direct sunlight.


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

Do Not Use

Do not use as a diaper, on children less than 2 months of age, or on open skin wounds. When using this product do not use in or near eyes. If contact occurs, flush thoroughly with water.

Otc - When Using

When using this product do not use in or near eyes. If contact occurs, flush thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.


  • Remove wipeWet hands thoroughly with wipe and allow hands to dry without wipingSupervise children under 6 years of age when using this product to avoid swallowing.

Inactive Ingredients

Aloe Barbadensis Leaf Extract,* Althaea Officinalis Root Extract,* Avena Sativa (Oat) Kernel Extract,* Camellia Sinensis Leaf Extract,* Chammomilla Recutita (Matricaria) Flower Extract,* Cucumis Sativus (Cucumber) Fruit Extract,* Glycerin, Lavandula Angustifolia(Lavender)Oil,Water.*Organic ingredients

Recent Major Changes

Indications and Usage: Hand Sanitizer to help reduce bacteria that potentially can cause disease. Store in a cool, dry place away from direct sunlight.Dosage and Administration: Supervise children under 6 years of age when using this product to avoid swallowing.Modified lanuage to include 99.9% effect against most common germsClarified list of germs this wipe is effective against (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Klebsiella and more")

* Please review the disclaimer below.