NDC 71611-017 Wish Ultra Alcohol Sanitizing Fresh Linen And Lilac

Ethyl Alcohol

NDC Product Code 71611-017

NDC 71611-017-55

Package Description: 550 mL in 1 BOTTLE

NDC Product Information

Wish Ultra Alcohol Sanitizing Fresh Linen And Lilac with NDC 71611-017 is a a human over the counter drug product labeled by Click Products Llc. The generic name of Wish Ultra Alcohol Sanitizing Fresh Linen And Lilac is ethyl alcohol. The product's dosage form is spray and is administered via topical form.

Labeler Name: Click Products Llc

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.

Wish Ultra Alcohol Sanitizing Fresh Linen And Lilac 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.

  • PROPANE (UNII: T75W9911L6)

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: 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: 09-26-2020 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.

Wish Ultra Alcohol Sanitizing Fresh Linen And Lilac Product Label Images

Wish Ultra Alcohol Sanitizing Fresh Linen And Lilac 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 Ingredients

Ethyl Alcohol 75%




-hand sanitizer to decrease bacteria on the skin-recommended for repeated use-for use when soap and water are not available


-Flammable.Keep away from heat and flame/fire-Keep away from heat, hot surfaces, open flames and ignition sources-Pressurized container. Do not pierce or burn even after use-Protect from sunlight-For external use only

Otc - Do Not Use

-On children less than 2 months of age-On open skin wounds

Otc - When Using

-Avoid use on/or around eyes, ears, mouth, broken/irritated skin or large areas of body. in case of contact with eyes, rinse thoroughly with water several minutes.- Do not inhale

Otc - Stop Use

-irritation persist-if product is swallowed

Otc - Keep Out Of Reach Of Children

If swallowed get medical help or contact a poison control center right away


-Shake well before use.-Hold can upright at 6-7 inches away from the surface and spray evenly.-Allow to air dry for 5 to 10 minutes. Repeat application a necessary.-Supervise children under 6 years of age when using this product to avoid swallowing.

Storage And Handling

-store between 15-30 degree Celcius-Do not expose to temperature exceeding 50 degree celcius

Inactive Ingredient

Ethanol, Butane, Propane, Isobutane, Parfum.

* Please review the disclaimer below.