NDC 26052-423 Burts Bees Naturally Clean Hand Sanitizer


NDC Product Code 26052-423

NDC 26052-423-01

Package Description: 59.1 mL in 1 BOTTLE, SPRAY

NDC Product Information

Burts Bees Naturally Clean Hand Sanitizer with NDC 26052-423 is a a human over the counter drug product labeled by Burt's Bees, Inc. The generic name of Burts Bees Naturally Clean Hand Sanitizer is alcohol. The product's dosage form is solution and is administered via topical form.

Labeler Name: Burt's Bees, Inc

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

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.

Burts Bees Naturally Clean Hand Sanitizer 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 66 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.

  • WITCH HAZEL (UNII: 101I4J0U34)
  • 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: Burt's Bees, Inc
Labeler Code: 26052
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: 12-31-2020 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.

Burts Bees Naturally Clean Hand Sanitizer Product Label Images

Burts Bees Naturally Clean 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

Active Ingredient(S)

Ethyl Alcoho 66% w/w. Purpose: Antiseptic


Antiseptic, Hand Sanitizer


For hand washing to decrease bacteria on the skin when water is not available.


For external use only. Flammable. Keep away from heat and open flame.

Do Not Use

  • In or near eyesin children less than 2 months of ageon deep puncture woulds; consult your doctor

Otc - When Using

When using this product Do not use in or near eyes.Disconinue use if irritaiton and redness developDo not use on deep puncture woulds: consult your doctor

Otc - Stop Use

Stop use if irritation or rash occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.


  • Apply liberally to unsoiled hands and rub thoroughlyAllow to dry witihout wiping or rinsing

Other Information

Stoer at room temperature

Inactive Ingredients

Glycerin, hamamelis virginiana(witch hazel) water, purified water USP

* Please review the disclaimer below.