NDC 67777-010 Sannytize Hand Sanitizer

Hand Sanitizer

NDC Product Code 67777-010

NDC 67777-010-01

Package Description: 144 BOX in 1 CASE > 24 BOTTLE in 1 BOX > 29.5 mL in 1 BOTTLE

NDC 67777-010-02

Package Description: 144 BOX in 1 CASE > 24 BOTTLE in 1 BOX > 59 mL in 1 BOTTLE

NDC 67777-010-03

Package Description: 96 BOX in 1 CASE > 24 BOTTLE in 1 BOX > 118.3 mL in 1 BOTTLE

NDC 67777-010-04

Package Description: 48 BOTTLE in 1 CASE > 236.5 mL in 1 BOTTLE

NDC 67777-010-05

Package Description: 12 BOTTLE, PUMP in 1 CASE > 473 mL in 1 BOTTLE, PUMP

NDC 67777-010-06

Package Description: 1728 BOX in 1 CASE > 144 PACKET in 1 BOX > 1.01 mL in 1 PACKET

NDC Product Information

Sannytize Hand Sanitizer with NDC 67777-010 is a a human over the counter drug product labeled by Dynarex Corporation. The generic name of Sannytize Hand Sanitizer is hand sanitizer. The product's dosage form is gel and is administered via topical form.

Labeler Name: Dynarex Corporation

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.

Sannytize 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 70 mL/100mL

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.

  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • WATER (UNII: 059QF0KO0R)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)

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.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Dynarex Corporation
Labeler Code: 67777
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: 11-01-2019 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: 12-31-2020 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.

Sannytize Hand Sanitizer Product Label Images

Sannytize 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

Ethyl Alcohol 70%

Purpose

Antiseptic Handwash

Use

  • For hand washing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

For external use only Flammable. Keep away from fire or flame

Do Not Use

In the eyes.

When Using This Product

Avoid contact with eyes. In case of eye contact, rinse with water to remove.

Stop Use And Ask A Doctor If

Irritation and redness develop.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Wet hands thoroughly with product and allow to dry without wiping

Other Information

  • Do not store above 110°FMay discolor some fabrics

Inactive Ingredients

Aloe Vera Leaf, Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked), Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine, Water

* Please review the disclaimer below.