NDC 70631-037 Thieves Waterless Hand Sanitizer


NDC Product Code 70631-037

NDC 70631-037-01

Package Description: 3 mL in 1 POUCH

NDC Product Information

Thieves Waterless Hand Sanitizer with NDC 70631-037 is a a human over the counter drug product labeled by Young Living Essential Oils, Lc.. The generic name of Thieves Waterless Hand Sanitizer is alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Young Living Essential Oils, Lc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Thieves Waterless 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 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.

  • WATER (UNII: 059QF0KO0R)
  • CLOVE OIL (UNII: 578389D6D0)

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: Young Living Essential Oils, Lc.
Labeler Code: 70631
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: 05-20-2021 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: 12-31-2022 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.

Thieves Waterless Hand Sanitizer Product Label Images

Thieves Waterless 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

Ethyl alcohol 65%




  • Helps reduce bacteria on the skinRecommended for repeated use


For external use onlyFlammable; keep away from fire or flame

When Using This Product

  • Keep out of eyesIn case of contact with eyes, flush thoroughly with waterAvoid contact with broken skin

Stop Use And Ask A Doctor If

Irritation  and redness develop and persist for more than 72 hours.

Keep Out Of Reach Of Children.

If swallowed get medical help or contact a Poison Control Center immediately.


  • Dispense directly on hands and rub in thoroughly For children under 6, use adult supervisionNot recommended for infants

Other Information

  • Close cap after each useDo not store above 104°F/40°C.

Inactive Ingredients

Water, Aloe vera leaf, Glycerin, Hydroxypropyl cellulose, Peppermint oil, Clove oil, Lemon oil, Eucalyptus radiata leaf oil, Rosemary oil, Cinnamon bark oil 100 pure, therapeuti-grade essential oil




* Please review the disclaimer below.