NDC 78089-045 Sanitol London Sanitizing

NDC Product Code 78089-045

NDC CODE: 78089-045

Proprietary Name: Sanitol London Sanitizing 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.

NDC Code Structure

  • 78089 - Endeks Kimya Sanayi Ve Ticaret Anonim Sirketi

NDC 78089-045-01

Package Description: 600 mL in 1 BOTTLE, SPRAY

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

NDC Product Information

Sanitol London Sanitizing with NDC 78089-045 is a product labeled by Endeks Kimya Sanayi Ve Ticaret Anonim Sirketi. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 2286295.

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)

Product Labeler Information

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

Labeler Name: Endeks Kimya Sanayi Ve Ticaret Anonim Sirketi
Labeler Code: 78089
Start Marketing Date: 09-04-2020 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Sanitol London Sanitizing Product Label Images

Sanitol London Sanitizing 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 decrease bacteria on the skin• recommended for repeated use• for use when soap and water are not available


• 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 woundsWhen using this product • Avoid use on/or around eyes, ears, mouth, broken/irritated skin or largeareas of body. In case of contact with eyes, rinse thoroughly with water several minutes. • do notinhale or ingest.Stop and ask doctor if• irritation persist• or if product is swallowed

Otc - Keep Out Of Reach Of Children

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 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/122 F.

Inactive Ingredients

Butane, Propane, Isobutane, Parfum, Glycerin

* Please review the disclaimer below.