NDC 56136-216 On The Go Hand Sanitizer Vanilla Vibes With Vitamin E

Alcohol

NDC Product Code 56136-216

NDC CODE: 56136-216

Proprietary Name: On The Go Hand Sanitizer Vanilla Vibes With 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

  • 56136 - Ganzhou Olivee Cosmetic Co., Ltd.
    • 56136-216 - On The Go Hand Sanitizer Vanilla Vibes

NDC 56136-216-01

Package Description: 10 mL in 1 BOTTLE, SPRAY

NDC Product Information

On The Go Hand Sanitizer Vanilla Vibes With Vitamin E with NDC 56136-216 is a a human over the counter drug product labeled by Ganzhou Olivee Cosmetic Co., Ltd.. The generic name of On The Go Hand Sanitizer Vanilla Vibes With Vitamin E is alcohol. The product's dosage form is spray and is administered via topical form.

Labeler Name: Ganzhou Olivee Cosmetic Co., Ltd.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

On The Go Hand Sanitizer Vanilla Vibes With 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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)

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: Ganzhou Olivee Cosmetic Co., Ltd.
Labeler Code: 56136
FDA Application Number: part333E 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: 09-25-2020 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.

On The Go Hand Sanitizer Vanilla Vibes With Vitamin E Product Label Images

On The Go Hand Sanitizer Vanilla Vibes With 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

Active Ingredient

Alcohol 70% w/w

Purpose

Antiseptic

Use

Antiseptic Cleanser, Help decrease bacteria on skin.

Warnings

For external use only.Flammable.Keep product away from fire or flame.When using this productavoid contact with eyes; in case of contact, flush eyes with water.Stop use and ask a doctor ifirritation or redness develops and persists.

Keep Out Of Reach Of Children.

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

Directions

  • Spray enough product on your palm to thoroughly cover your hads. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

Water (Aqua), Glycerin, Fragrance (Parfum), Aloe Barbadensis Leaf Extract, Tocopheryl, Actate (Vitamin E).

* Please review the disclaimer below.