NDC 75186-007 Primeauty Instant Hand Sanitizer

Ethyl Alcohol

NDC Product Code 75186-007

NDC 75186-007-01

Package Description: 10 mL in 1 TUBE

NDC 75186-007-02

Package Description: 20 mL in 1 TUBE

NDC 75186-007-03

Package Description: 30 mL in 1 TUBE

NDC 75186-007-04

Package Description: 50 mL in 1 TUBE

NDC 75186-007-05

Package Description: 60 mL in 1 TUBE

NDC 75186-007-06

Package Description: 80 mL in 1 TUBE

NDC 75186-007-07

Package Description: 100 mL in 1 TUBE

NDC 75186-007-08

Package Description: 150 mL in 1 TUBE

NDC 75186-007-09

Package Description: 200 mL in 1 TUBE

NDC 75186-007-10

Package Description: 30 mL in 1 BOTTLE

NDC 75186-007-11

Package Description: 50 mL in 1 BOTTLE

NDC 75186-007-12

Package Description: 60 mL in 1 BOTTLE

NDC 75186-007-13

Package Description: 80 mL in 1 BOTTLE

NDC 75186-007-14

Package Description: 100 mL in 1 BOTTLE

NDC 75186-007-15

Package Description: 150 mL in 1 BOTTLE

NDC 75186-007-16

Package Description: 200 mL in 1 BOTTLE

NDC 75186-007-17

Package Description: 250 mL in 1 BOTTLE

NDC 75186-007-18

Package Description: 240 mL in 1 BOTTLE, PUMP

NDC 75186-007-19

Package Description: 250 mL in 1 BOTTLE, PUMP

NDC 75186-007-20

Package Description: 300 mL in 1 BOTTLE, PUMP

NDC 75186-007-21

Package Description: 350 mL in 1 BOTTLE, PUMP

NDC 75186-007-22

Package Description: 400 mL in 1 BOTTLE, PUMP

NDC 75186-007-23

Package Description: 500 mL in 1 BOTTLE, PUMP

NDC 75186-007-24

Package Description: 1000 mL in 1 BOTTLE, PUMP

NDC 75186-007-25

Package Description: 1000 mL in 1 DRUM

NDC 75186-007-26

Package Description: 2000 mL in 1 DRUM

NDC 75186-007-27

Package Description: 4000 mL in 1 DRUM

NDC 75186-007-28

Package Description: 5000 mL in 1 DRUM

NDC 75186-007-29

Package Description: 10000 mL in 1 DRUM

NDC 75186-007-30

Package Description: 15000 mL in 1 DRUM

NDC 75186-007-31

Package Description: 20000 mL in 1 DRUM

NDC 75186-007-32

Package Description: 25000 mL in 1 DRUM

NDC 75186-007-33

Package Description: 50000 mL in 1 DRUM

NDC Product Information

Primeauty Instant Hand Sanitizer with NDC 75186-007 is a a human over the counter drug product labeled by Huizhou Duomei Daily Necessites Co.,ltd. The generic name of Primeauty Instant Hand Sanitizer is ethyl alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Huizhou Duomei Daily Necessites 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.

Primeauty 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/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.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
  • WATER (UNII: 059QF0KO0R)
  • ALOE (UNII: V5VD430YW9)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

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: Huizhou Duomei Daily Necessites Co.,ltd
Labeler Code: 75186
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: 08-28-2020 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.

Primeauty Instant Hand Sanitizer Product Label Images

Primeauty 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% v/v

Purpose

Antiseptic

Use

  • For hand washing to decrease bacteria on the skin.Recommended for repeated use.

Warnings

For external use only.Flammable, keep away from heat and flame.

Do Not Use

Do not use in the eyes, in case of contact, rinse eyes thoroughly with water.Do not use on children less than 2 months of age.

Stop Use And Ask A Doctor If

  • Irritation and redness develop and persist for more than 72 hours.Swallowed, get medical help or contact a posion control center right away.

Keep Out Of Reach Of Children

Children must be supervised in use of this product.

Directions

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

Other Information

  • Store below 110F (43C)May discolor certian fabrics or surfaces.

Inactive Ingredients

Aqua(Water),Glycerin,Carbomer,Triethanolamine, Fragrance,Aloe,Tocopheryl Acetate (Vitamin E)

* Please review the disclaimer below.