NDC 76922-938 Lavender Sanimoist Hand Sanitizer
Benzalkonium Chloride Lotion Topical

Product Information

What is NDC 76922-938?

The NDC code 76922-938 is assigned by the FDA to the product Lavender Sanimoist Hand Sanitizer which is a human over the counter drug product labeled by Trigg Laboratories D/b/a Wet International. The generic name of Lavender Sanimoist Hand Sanitizer is benzalkonium chloride. The product's dosage form is lotion and is administered via topical form. The product is distributed in 4 packages with assigned NDC codes 76922-938-04 118.3 ml in 1 bottle , 76922-938-10 10 ml in 1 pouch , 76922-938-16 474 ml in 1 bottle , 76922-938-32 947 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code76922-938
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Lavender Sanimoist Hand Sanitizer
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Benzalkonium Chloride
Product Type 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.
Human Otc Drug
Dosage FormLotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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.
  • 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.
Trigg Laboratories D/b/a Wet International
Labeler Code76922
FDA Application Number 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 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.
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date 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 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 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".
NDC Code Structure

What are the uses for Lavender Sanimoist Hand Sanitizer?

Product Packages

NDC Code 76922-938-04

Package Description: 118.3 mL in 1 BOTTLE

NDC Code 76922-938-10

Package Description: 10 mL in 1 POUCH

NDC Code 76922-938-16

Package Description: 474 mL in 1 BOTTLE

NDC Code 76922-938-32

Package Description: 947 mL in 1 BOTTLE

Product Details

What are Lavender Sanimoist Hand Sanitizer Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Lavender Sanimoist Hand Sanitizer Active Ingredients UNII Codes

Lavender Sanimoist Hand Sanitizer Inactive Ingredients UNII Codes

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.

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Lavender Sanimoist Hand Sanitizer Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents

Otc - Active Ingredient

Active Ingredients

Benzalkonium Chloride 0.13%

Otc - Purpose



Indications & Usage


  • Hand Sanitizer to decrease bacteria on the skin.
  • Recommended for repeat use.



• For external use only: Hands

Do not use on

  • irritated or broken skin
  • When using this product

    • Avoid contact with eyes
    • In case of eye contact, flush with water

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

  • If swallowed, get medical help.
  • Discontinue use

    • If skin irritation or redness develops

Dosage & Administration


  • Apply liberally to hands, and massage into skin.
  • Reapply as necessary
  • For children under 6, use only under adult supervision.


Other information
Do not use if tamper evident seal is removed or broken.

Distributed By

Trigg Laboratories, Inc.
4220 W Windmill Ln Suite 140,
Las Vegas, NV 89139
Made in the USA

Inactive Ingredient

Inactive Ingredients

Purified Water, PEG-6 (and) AMP-Acrylates/Vinyl, Cetearyl Alcohol, Coconut Glycerin, Propanediol, Caprylic/Capric Triglycerides, Fragrance, Phenoxyethanol, Sesamum Indicum (Sesame) Oil, Aloe Barbadensis (Aloe) Leaf Juice, Tocopheryl Acetate, Mentha Spicata (Mint) Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Lavandula Angustifolia (Lavender) Flower Extract.

Otc - Questions

+1 (866) 233-8898

Principal Display Panel

NDC 76922-938-32

Lavender Sanimoist Hand Sanitizer

2 IN 1 Moisturizing Cream Hand Sanitizer

Kills 99.9% of  Germs

No Drying Alcohol


32 Fl. Oz. US/ 947 mL e

* Please review the disclaimer below.