NDC 73344-108 Amoray Premium Instant Hand Sanitizer With Aloe And Vitamin E Original

Alcohol

NDC Product Code 73344-108

NDC Code: 73344-108

Proprietary Name: Amoray Premium Instant Hand Sanitizer With Aloe And Vitamin E Original 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

  • 73344 - Ningbo Sante Ying Medicaland Healthdevelopment Co.,ltd
    • 73344-108 - Amoray Premium Instant Hand Sanitizer With Aloe And Vitamin E

NDC 73344-108-01

Package Description: 53 mL in 1 BOTTLE

NDC Product Information

Amoray Premium Instant Hand Sanitizer With Aloe And Vitamin E Original with NDC 73344-108 is a a human over the counter drug product labeled by Ningbo Sante Ying Medicaland Healthdevelopment Co.,ltd. The generic name of Amoray Premium Instant Hand Sanitizer With Aloe And Vitamin E Original is alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Ningbo Sante Ying Medicaland Healthdevelopment 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.

Amoray Premium Instant Hand Sanitizer With Aloe And Vitamin E Original 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/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, D- (UNII: A7E6112E4N)
  • 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.

Product Labeler Information

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

Labeler Name: Ningbo Sante Ying Medicaland Healthdevelopment Co.,ltd
Labeler Code: 73344
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: 09-29-2019 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.

Amoray Premium Instant Hand Sanitizer With Aloe And Vitamin E Original Product Label Images

Amoray Premium Instant Hand Sanitizer With Aloe And Vitamin E Original 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                62%      ...        Antimicrobial

Otc - Purpose

Hand sanitizer to help decrease bacteria on the skin that may cause disease.

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact local poison control center right away.Children must be supervised in use of this product.

Indications & Usage

Keep out of eyeswhen water, soap and towel are not available

Warnings

For external use only.Flammable. Keep away from hear or flame.
Do not apply around eyes; Do not use in ears and mouth. When using this
products, avoid contact with eyes. In case of contact, flush eyes with
water.Stop using and ask a doctor, if irritation and redness develops, if condition persists for more than 72 hours, consult a doctor.

Dosage & Administration

Pump as needed into your palms and thoroughly spread on both hands, and rub the skin until dry. Children under 6 years of age should be supervised by an adult when using.

Inactive Ingredient

Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), Fragrance

* Please review the disclaimer below.