NDC 77418-306 Abutol Sanitizing White Lilac

Product Information

Product Code77418-306
Proprietary Name 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.
Abutol Sanitizing White Lilac
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Atak Farma Kozmetik Ve Kimya Sanayi Ticaret Anonim Sirketi
Labeler Code77418
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
10-23-2020
Listing Expiration Date 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.
12-31-2021
Exclude Flag 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".
I
NDC Code Structure

Usage Information


Product Packages

NDC 77418-306-50

Package Description: 550 mL in 1 BOTTLE, SPRAY

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

Product Details

Abutol Sanitizing White Lilac is product labeled by Atak Farma Kozmetik Ve Kimya Sanayi Ticaret Anonim Sirketi. The product's dosage form is and is administered via form.


What are Abutol Sanitizing White Lilac Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL (UNII: 3K9958V90M)
  • ALCOHOL (UNII: 3K9958V90M) (Active Moiety)


NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:


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.

  • BUTANE (UNII: 6LV4FOR43R)
  • PROPANE (UNII: T75W9911L6)
  • ISOBUTANE (UNII: BXR49TP611)
  • GLYCERIN (UNII: PDC6A3C0OX)


* Please review the disclaimer below.

Abutol Sanitizing White Lilac Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Drug Facts




Active Ingredient



Ethyl alcohol 75%


Purpose



Antiseptic


Uses



hand sanitizer to decrease bacteria on the skin

recommended for repeated use

for use when soap and water are not available


Warnings



Extremely flammable aerosol, keep away from fire / flame.

Keep away from heat, hot surfaces, open flames and other ignition sources.

Pressurized container. Do not pierce or burn even after use.

Protect from the sunlight.

For external use only

Do not use

on children less than 2 months of age

on open skin wounds

When using this product  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 or ingest

Stop and ask doctor if

irritation persist

or if product is swallowed


Keep Out Of Reach Of Children.



If swallowed get medical help or contact a Poison Control Center right away.


Directions



Shake well before use.

Hold can upright at 6-7 inches away from 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


Other Information



store between 15-30°C (59-86°F)

Do not expose to temperatures exceeding 50 C/122F.


Inactive Ingredients



Butane, Propane, Isobutane, Glycerin, Parfum


Packaging




* Please review the disclaimer below.