NDC 76922-938 Lavender Sanimoist Hand Sanitizer

Lavender Sanimoist Hand Sanitizer with NDC 76922-938 is a 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.

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.

Lavender Sanimoist Hand Sanitizer Active Ingredient(s)

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

Inactive Ingredient(s)

• 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)

• 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

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 ("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".

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