NDC 71611-032 Wish/ Wish Ultra Slim Hand Sanitizer

Ethyl Alcohol

NDC Product Code 71611-032

NDC CODE: 71611-032

Proprietary Name: Wish/ Wish Ultra Slim Hand Sanitizer 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: Ethyl 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.

Product Characteristics

PURPLE (C48327)

NDC Code Structure

NDC 71611-032-01

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC 71611-032-02

Package Description: 90 mL in 1 BOTTLE, PLASTIC

NDC 71611-032-03

Package Description: 20 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Wish/ Wish Ultra Slim Hand Sanitizer with NDC 71611-032 is a a human over the counter drug product labeled by Click Products Llc. The generic name of Wish/ Wish Ultra Slim Hand Sanitizer is ethyl alcohol. The product's dosage form is liquid and is administered via topical form.

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.

Wish/ Wish Ultra Slim 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.

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.

  • D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
  • CARBOMER 940 (UNII: 4Q93RCW27E)
  • 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.

Product Labeler Information

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

Labeler Name: Click Products Llc
Labeler Code: 71611
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: 04-25-2020 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 - NO 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.

Wish/ Wish Ultra Slim Hand Sanitizer Product Label Images

Wish/ Wish Ultra Slim 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

Hand Sanitizer

Kills 99.9% of germs

Active Ingredient

Active Ingredient PurposeEthyl Alcohol 75% v/v Antimicrobial


Reduce bacteria and viruses onthe hands that may cause disease.


For external use only.


Keep away from heat and flame.

When Using This Product

Avoid contact with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop And Ask A Doctor If

Irritation or redness develops.

Keep Out Of Reach Of Children.

If swallowed get immediate medical help or contact a poison contaol center right away.

Indications & Usage


Dosage & Administration

Wet hands thoroughly with product and rub into skin until dry.

User Safety Warnings

Children under 6 years of age should be supervised by an adult when using.

Inactive Ingredients:

Water( aqua), Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance, Aloe Barbadensis( Aloe Vera) Gel, Tocopheryl acetate( vitamin E), D&C Violet No. 2.

* Please review the disclaimer below.