NDC 17307-1117 Hand Sanitizer Gel

Alcohol

NDC Product Code 17307-1117

NDC 17307-1117-1

Package Description: 118.29 mL in 1 BOTTLE, PLASTIC

NDC 17307-1117-2

Package Description: 354.88 mL in 1 BOTTLE

NDC 17307-1117-3

Package Description: 3780 mL in 1 JUG

NDC 17307-1117-6

Package Description: 208198 mL in 1 DRUM

NDC 17307-1117-7

Package Description: 1003025 mL in 1 CONTAINER

NDC 17307-1117-8

Package Description: 499.79 mL in 1 BOTTLE, PUMP

NDC 17307-1117-9

Package Description: 59.147 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Hand Sanitizer Gel with NDC 17307-1117 is a a human over the counter drug product labeled by Agrochem Inc. The generic name of Hand Sanitizer Gel is alcohol. The product's dosage form is solution and is administered via topical form.

Labeler Name: Agrochem Inc

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

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 Gel 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 .7 mL/mL

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: Agrochem Inc
Labeler Code: 17307
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: 09-21-2020 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.

Hand Sanitizer Gel Product Label Images

Hand Sanitizer Gel 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, Hand SanitizerAntimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin that could cause disease Recommended for repeated use.

Warnings

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

Do Not Use

  • In children less than 2 months of ageon open skin wounds

Otc - When Using

When using this product do not use in or near the eyes. When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Otc - Stop Use

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dryNo rinsing requiredNo towels needed.

Other Information

Do not store above 110°F (43°C). May discolor certain fabrics or surfaces.

Inactive Ingredients

Water (Aqua), Aloe Vera, Propylene Glycol, Carboxethyl Acrylate Crosspolymer, Fragrance, FD&C Blue #1, FD&C Yellow #5

Description

Hand Sanitizer GelMoisturizing with AloeEffective at eliminating more than 99.9% of many common harmful germs & bacteria in as little as 15 seconds.

* Please review the disclaimer below.