NDC 76922-936 Unscented Sanimoist Hand Sanitizer

Benzalkonium Chloride

NDC Product Code 76922-936

NDC 76922-936-04

Package Description: 118.3 mL in 1 BOTTLE

NDC 76922-936-10

Package Description: 10 mL in 1 POUCH

NDC 76922-936-16

Package Description: 474 mL in 1 BOTTLE

NDC 76922-936-32

Package Description: 947 mL in 1 BOTTLE

NDC Product Information

Unscented Sanimoist Hand Sanitizer with NDC 76922-936 is a a human over the counter drug product labeled by Trigg Laboratories D/b/a Wet International. The generic name of Unscented Sanimoist Hand Sanitizer is benzalkonium chloride. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Trigg Laboratories D/b/a Wet International

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

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.

Unscented Sanimoist 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.

  • BENZALKONIUM CHLORIDE .13 g/mL
  • BENZALKONIUM CHLORIDE .13 g/mL
  • BENZALKONIUM CHLORIDE .13 g/mL
  • BENZALKONIUM CHLORIDE .13 g/mL

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • SESAME OIL (UNII: QX10HYY4QV)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • SPEARMINT (UNII: J7I2T6IV1N)
  • ROSEMARY (UNII: IJ67X351P9)
  • LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)

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.

Labeler Name: Trigg Laboratories D/b/a Wet International
Labeler Code: 76922
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: 03-01-2021 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: 12-31-2022 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Unscented Sanimoist Hand Sanitizer Product Label Images

Unscented Sanimoist 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

Otc - Active Ingredient

Active IngredientsBenzalkonium Chloride 0.13%

Otc - Purpose

PurposeAntimicrobial

Indications & Usage

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

Warnings

  • Warnings • For external use only: Hands
  • Do not use onirritated or broken skinWhen using this productAvoid contact with eyesIn 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 useIf skin irritation or redness develops

Dosage & Administration

  • DirectionsApply liberally to hands, and massage into skin.Reapply as necessaryFor children under 6, use only under adult supervision.

Other

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

Distributed ByTrigg Laboratories, Inc.


4220 W Windmill Ln Suite 140,


Las Vegas, NV 89139


Made in the USA

Inactive Ingredient

Inactive IngredientsPurified Water, PEG-6 (and) AMP-Acrylates/Vinyl, Coconut Glycerin, Propanediol, Phenoxyethanol, Caprylic/Capric Triglycerides, Cetearyl Alcohol, 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

Questions?+1 (866) 233-8898

* Please review the disclaimer below.