NDC 74149-003 Hand Safe Hand Sanitizer Advanced Aloe Vera Vitamin E

Alcohol

NDC Product Code 74149-003

NDC CODE: 74149-003

Proprietary Name: Hand Safe Hand Sanitizer Advanced Aloe Vera Vitamin E What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Alcohol What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 74149 - Yiwu Yangjie Daily Chemicals Co.,ltd.

NDC 74149-003-01

Package Description: 59 mL in 1 BOTTLE

NDC 74149-003-02

Package Description: 236 mL in 1 BOTTLE

NDC Product Information

Hand Safe Hand Sanitizer Advanced Aloe Vera Vitamin E with NDC 74149-003 is a a human over the counter drug product labeled by Yiwu Yangjie Daily Chemicals Co.,ltd.. The generic name of Hand Safe Hand Sanitizer Advanced Aloe Vera Vitamin E is alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Yiwu Yangjie Daily Chemicals Co.,ltd.

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 Safe Hand Sanitizer Advanced Aloe Vera Vitamin E 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.

  • WATER (UNII: 059QF0KO0R)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CARBOMER 934 (UNII: Z135WT9208)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • TROLAMINE (UNII: 9O3K93S3TK)

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: Yiwu Yangjie Daily Chemicals Co.,ltd.
Labeler Code: 74149
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: 05-02-2020 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 Safe Hand Sanitizer Advanced Aloe Vera Vitamin E Product Label Images

Hand Safe Hand Sanitizer Advanced Aloe Vera Vitamin E 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

Otc - Active Ingredient

Active ingredient                                  PurposeEthyl Alcohol                70%  V/V    ...   Antiseptic

Otc - Purpose

  • Help decrease bacteria on the hands.recommended for repeated use.

Otc - Keep Out Of Reach Of Children

If swallowed, get meical help or contact a poison control center right away.

Indications & Usage

Dispense a small amount on palms. Rub lightly until dry. Do not rinse.

Warnings

For external use only.Flammable. Keep away from fire or flame.Avoid contact with eyes, in case of contact, rinse with water immediately.If irritation develops, discontinue use and consult a doctor.OTHER INFORMATION: store under 105℉.

Dosage & Administration

Dispense a small amount on palms. Rub lightly until dry. Do not rinse.

Inactive Ingredient

Water (Aqua), Glycerin, Pollyacrylic Acid, Aminomethyl Propanol, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract

* Please review the disclaimer below.