NDC 42869-802 Freeman Packaging Hand Sanitizer

NDC Product Code 42869-802

NDC CODE: 42869-802

Proprietary Name: Freeman Packaging 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

  • 42869 - Jiangmen Nowadays Daily Goods Co., Ltd.

NDC 42869-802-01

Package Description: 7.5 mL in 1 BOTTLE

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

NDC Product Information

Freeman Packaging Hand Sanitizer with NDC 42869-802 is a product labeled by Jiangmen Nowadays Daily Goods Co., Ltd.. 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: 581660.

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.

  • 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: Jiangmen Nowadays Daily Goods Co., Ltd.
Labeler Code: 42869
Start Marketing Date: 08-28-2015 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: 12-31-2017 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.

Freeman Packaging Hand Sanitizer Product Label Images

Freeman Packaging 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

Ethyl Alcohol 62%




  • To decrease bacteria on the skin that could cause diseaserecommended for repeated use


For external use only- hands.Flammable. Keep away from heat and flame.When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water.Avoid contact with broken skin.Do not inhale or ingest.Stop use and ask a doctor if skin irritation develops.

When Using This Product

  • Keep out of eyes. In case of contact with eyes, immediately flush with water and call a doctor.avoid contact with broken skin.

Stop Use And Ask A Doctor

If irritation or redness develops

Keep Out Of Reach Of Children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.


  • Wet hands thoroughly with product and allow to dry without wipingfor children under 6, use only under adult supervisionnot recommended for infants

Other Information

  • Do not store above 105Fmay discolor some babricsharmful to wood finishes and plastics

Inactive Ingredients

Aloe vere gel, extracts of juniper, eucalyptus oil, carbomer, thymol essence (radix), diisoprpanol amine, triethanolamine, water.

* Please review the disclaimer below.