NDC 42681-0002 Hand Sanitizer Peppermint Vanilla

Ethyl Alcohol

NDC Product Code 42681-0002

NDC 42681-0002-1

Package Description: 30 mL in 1 BOTTLE

NDC Product Information

Hand Sanitizer Peppermint Vanilla with NDC 42681-0002 is a a human over the counter drug product labeled by Whole Foods Market, Inc.. The generic name of Hand Sanitizer Peppermint Vanilla is ethyl alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Whole Foods Market, Inc.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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 Sanitizer Peppermint Vanilla 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 62 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.

  • WATER (UNII: 059QF0KO0R)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
  • CHIA SEED OIL (UNII: MC2LH51BO7)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • ROSEMARY (UNII: IJ67X351P9)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)

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: Whole Foods Market, Inc.
Labeler Code: 42681
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: 06-08-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 06-08-2025 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Hand Sanitizer Peppermint Vanilla Product Label Images

Hand Sanitizer Peppermint Vanilla 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

Otc - Active Ingredient

Active Ingredient Ethyl Alcohol 62% v/v

Otc - Purpose

Purpose Antiseptic

Warnings

For external use only. Flammable. Keep away from fire or flame.

Otc - When Using

When using this product avoid contact with eyes. If eye contact occurs, rinse with water.

Otc - Stop Use

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

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

Indications & Usage

Uses to help reduce bacteria on the skin

Dosage & Administration

Directions apply enough gel to wet hands and rub together until dry. Use 1 to 3 times daily.

Storage And Handling

Other information do not store above 104°F (40°C).

Otc - Questions

Questions, Comments?customer.questions@wholefoods.com1-844-963-8255

Inactive Ingredient

Inactive ingredients water, isopropyl alcohol, hydroxyethylcellulose, fragrance (natural)*, glycerin, salvia hispanica (chia) seed oil, helianthus annuus (sunflower) seed oil, rosmarinus officinalis (rosemary) extract.

* Please review the disclaimer below.