NDC 51706-965 Hand Sanitizer Sweet Peach Citrus


NDC Product Code 51706-965

NDC 51706-965-01

Package Description: 28 mL in 1 BOTTLE

NDC Product Information

Hand Sanitizer Sweet Peach Citrus with NDC 51706-965 is a a human over the counter drug product labeled by Landy International. The generic name of Hand Sanitizer Sweet Peach Citrus is alcohol. The product's dosage form is gel and is administered via topical form.

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 Sweet Peach Citrus 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.

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)

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: Landy International
Labeler Code: 51706
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: 10-15-2021 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.

Hand Sanitizer Sweet Peach Citrus Product Label Images

Hand Sanitizer Sweet Peach Citrus 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(S)

Alcohol 70%




Helps eliminate bacteria on hands when water is not available


For external use only

Flammable keep away from heat or flame.

Does not contain grainalcohol, do not drink.lf taken internally willproduce severe gastricdisturbances.

Do not use

On children less than 2months of age

oOn open skin woundsWhen using this productkeep out of eyes, ears, andmouth in case of contact witheyes, rinse eyes thouroughlywith water.

Stop use and ask a doctor if irritation or rash occurs this may be a sign of a serious conaton.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children,

●Except under adult supervision.lf swallowed, get medical helpor contact a Poison ControlCenter right away.


Place enough product on handsto cover all surfaces.

Rub hands together until dry.Supervise children under 6years of age when using thisproduct to avoid swallowing.Other information

Other Information

Store between 15-30C(59-86°F)

Avoid freezing and excessiveheat above 40°C (104°F)

Inactive Ingredients

Water(Aqua), Fragrance(Parfum),Acrylates/C10-30Alkyl Acrylate Crosspolymer,Glycerin, Triethanolamine

* Please review the disclaimer below.