NDC 77718-001 Yozio Perfect Hand Sanitizer Gel

NDC Product Code 77718-001

NDC CODE: 77718-001

Proprietary Name: Yozio Perfect Hand Sanitizer Gel 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.

NDC Code Structure

NDC 77718-001-01

Package Description: 45 mL in 1 TUBE

NDC 77718-001-02

Package Description: 50 mL in 1 TUBE

NDC 77718-001-03

Package Description: 60 mL in 1 TUBE

NDC 77718-001-04

Package Description: 100 mL in 1 BOTTLE, PUMP

NDC 77718-001-05

Package Description: 200 mL in 1 BOTTLE, PUMP

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Yozio Perfect Hand Sanitizer Gel with NDC 77718-001 is a product labeled by Yozo Cosmetic Co.,ltd. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 581660.

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)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
  • TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

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

Labeler Name: Yozo Cosmetic Co.,ltd
Labeler Code: 77718
Start Marketing Date: 05-13-2020 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Yozio Perfect Hand Sanitizer Gel Product Label Images

Yozio Perfect 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

Ethyl alcohol 62%

Purpose

Antimicrobial

Use

  • Hand sanitizer to help reduce bacteria on the skin

Warnings

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

Otc - When Using

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

Otc - Stop Use

Stop use and ask a doctor if irritation or rash appears and lasts

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

  • Put nough produt in your palm to cover hands and rub hands together briskly until dry.Children under 6 years of age should be supervised when using this product

Other Information

  • Store below 86°F (30°C)May discolor certain fabrics or surfaces

Inactive Ingredients

Water, Glycerin, Carbomer, Triethanolamine, Dipropylene Glycol

* Please review the disclaimer below.