NDC 70939-001 Hand Sanitizer

NDC Product Code 70939-001

NDC CODE: 70939-001

Proprietary Name: 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.

NDC Code Structure

  • 70939 - Dongguang Shuoguo Silicone Products Co., Ltd.

NDC 70939-001-01

Package Description: 200 POUCH in 1 PACKAGE > 30 mL in 1 POUCH

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

NDC Product Information

Hand Sanitizer with NDC 70939-001 is a product labeled by Dongguang Shuoguo Silicone Products Co., Ltd.. The product's dosage form is and is administered via form.

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.

  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CARBOMER 934 (UNII: Z135WT9208)
  • TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

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

Labeler Name: Dongguang Shuoguo Silicone Products Co., Ltd.
Labeler Code: 70939
Start Marketing Date: 08-31-2016 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.

Hand Sanitizer Product Label Images

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

Active Ingredient

Alcohol 63%

Purpose

Antiseptic Hand Sanitizer

Use

To decrease bacteria on the skin

Warnings

For external use onlyFlammable: Keep away from fire or flameAlcohol is usedDo not use in the eyes. If this happens, rinse thoroughly with water.In case of deep or puncture wounds, consult your doctorStop use and ask a doctor if irritation or redness develops and persists for more than 72 hours

Keep Out Of Reach Of Children

If swallowed

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

Directions

Liberally spray on skin and gently massage until absorbed

Inactive Ingredient

Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadenis Leaf, Fragrance, Carbomer

* Please review the disclaimer below.