NDC 68320-800 Symmetry Hand Sanitizer

Hand Sanitizer

NDC Product Code 68320-800

NDC 68320-800-02

Package Description: 1 PACKET in 1 BOX > .9 mL in 1 PACKET (68320-800-01)

NDC Product Information

Symmetry Hand Sanitizer with NDC 68320-800 is a a human over the counter drug product labeled by Orlandi Inc.. The generic name of Symmetry Hand Sanitizer is hand sanitizer. The product's dosage form is gel and is administered via topical form.

Labeler Name: Orlandi Inc.

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.

Symmetry 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 .62 mL/.9mL

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: Orlandi Inc.
Labeler Code: 68320
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: 12-30-2020 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: 12-31-2021 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 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.

Symmetry Hand Sanitizer Product Label Images

Symmetry 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(S)

Ethyl Alcohol 70% v/v. Purpose: Antiseptic


Antiseptic, Hand Sanitizer


Reduces bacteria on skin


Flammable. Keep away from heat or flame. For external use only. Do not use in or near the eyes. In case of contact rinse with water.

Do Not Use

Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

Otc - When Using

For external use only. Do not use in or near the eyes. In case of contact, rinse eyes throuighly with water. Stop use and consult a doctr if irritation occurs. Keep out of reach of children, If swallowed, get medical help or contact a Poison Control Center immediately.

Otc - Stop Use

Stop use and ask a doctor if irritation occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


  • Place enough product in your palm to throughly cover your hands and rub together until dry.Children under 6 years shoild be supervised when using this product.

Other Information

Store at temperature below 110F (43C)May discolor certain fabrics or surfaces.

Inactive Ingredients

Water, methyl alcohol, ammonium acrylodimethyltaurate/carboxethyl acrylate crosspolyme, glycerin, hydrogen peroxide.

Place Enough Product In Your Palm To Throughly Cover Your Hands And Rub Together Until Dry. Children Under 6 Years Should Be Supervised When Using This Product.

Use: Reduces bacteria on skin

* Please review the disclaimer below.