NDC 77985-001 Bioperfect Instant Hand Sanitizer


NDC Product Code 77985-001

NDC 77985-001-01

Package Description: 30 mL in 1 BOTTLE

NDC 77985-001-02

Package Description: 60 mL in 1 BOTTLE

NDC 77985-001-03

Package Description: 300 mL in 1 BOTTLE

NDC 77985-001-04

Package Description: 500 mL in 1 BOTTLE

NDC 77985-001-05

Package Description: 3785 mL in 1 BOTTLE

NDC Product Information

Bioperfect Instant Hand Sanitizer with NDC 77985-001 is a a human over the counter drug product labeled by Shandong Renrui Biotechnology Co, Ltd.. The generic name of Bioperfect Instant Hand Sanitizer is alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Shandong Renrui Biotechnology Co, Ltd.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Bioperfect Instant Hand Sanitizer 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 .75 mL/mL

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)

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: Shandong Renrui Biotechnology Co, Ltd.
Labeler Code: 77985
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: 07-10-2020 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.

Bioperfect Instant Hand Sanitizer 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 75%




  • Hand sanitizer to help decrease bacteria on the skin.when water, soap & towel are not available.recommended for repeated use


  • For external use only FlamableKeep away from fire or flame.

Do Not Apply Around Eyes. Do Not Use

In ears and mouth.

When Using This Product,

Avoid contact with eyes. In case of contact flush eyes with water.

Stop Use And Ask A Doctor

If redness or irritation develop and persist for more than 72 hours.

Keep Out Of Reach Of Children.

Children must be supervised in use of this product.


  • Pumps as needed into your palms and thoroughly spread on both hands.rub into skin until dry.

Other Information

  • Store at 20 °C (68 °to 77° F)may discolor fabrics

Inacive Ingredients

Water, Isopropyl alcohol, Carbomer, Triethanolamine, Glycerin, Tocopheryl Acetate, Aloe Vera Leaf Juice.

* Please review the disclaimer below.