NDC 79359-001 Sani Hands

NDC Product Code 79359-001

NDC CODE: 79359-001

Proprietary Name: Sani Hands 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

  • 79359 - Maine Craft Distilling, Llc

NDC 79359-001-16

Package Description: 60 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Sani Hands with NDC 79359-001 is a product labeled by Maine Craft Distilling, Llc. 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: 2277550.

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.

  • METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Maine Craft Distilling, Llc
Labeler Code: 79359
Start Marketing Date: 07-17-2020 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.

Sani Hands Product Label Images

Sani Hands 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 72%

Purpose

Antiseptic

Uses

Hand Sanitizer to help reduce bacteria on the skin that can cause disease.

Directions

Apply liberally to front and back of hands.Allow to dry. Recommended for repeat use.

Warnings

For external use only: handsFlammable, keep away from fire or flame.When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.Stop use and ask a doctor if irritation or redness appears and lasts.Do not use on children less than 2 months of age and on open wounds. Do not inhale or ingest.Supervise children under 6 years of age when using this product to avoid swallowing

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center immediately.

Other Information

Store between 0ºC (32ºF) - 41ºC (105ºF)

Inactive Ingredients

Methylcellulose, water, Fragrance

Customer Service

+1 800 960 4814

* Please review the disclaimer below.