NDC 49681-100 New Life Moisturizing Hand Sanitizer


NDC Product Code 49681-100

NDC 49681-100-01

Package Description: 30 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-02

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-04

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-05

Package Description: 4.44 mL in 1 POUCH

NDC 49681-100-10

Package Description: 59 mL in 1 TUBE

NDC 49681-100-11

Package Description: 331 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-14

Package Description: 420 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-16

Package Description: 473 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-20

Package Description: 52 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-29

Package Description: 858 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-32

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-40

Package Description: 112 mL in 1 BOTTLE, PLASTIC

NDC 49681-100-80

Package Description: 228 mL in 1 BOTTLE, PLASTIC

NDC Product Information

New Life Moisturizing Hand Sanitizer with NDC 49681-100 is a a human over the counter drug product labeled by New Life Products, Inc.. The generic name of New Life Moisturizing Hand Sanitizer is ethanol. The product's dosage form is gel and is administered via topical form.

Labeler Name: New Life Products, Inc.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

New Life Moisturizing Hand Sanitizer Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 70 mL/100mL

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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: New Life Products, Inc.
Labeler Code: 49681
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-27-2020 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: 12-31-2022 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: N - NO 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.

New Life Moisturizing Hand Sanitizer Product Label Images

New Life Moisturizing 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

Ethanol 70%



Indications & Usage

Uses • Hand sanitizer to decrease bacteria on skin • Recommended for repeated use


Warning • For external use onlyFlammable. Keep away from fire or flame.When using this product avoid contact with face, eyes and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advice.Stop use and ask doctor if irritation and redness develops.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Dosage & Administration

Directions • Wet hands thoroughly with product and rub into skin until dry. • Children under 6 years of age should be supervised by an adult when using this product.

Inactive Ingredient

Inactive Ingredients: Water (Aqua), Polysorbate 20, Isopropyl Alcohol, Tocopheryl Acetate, Panthenol, Methyl Gluceth-20, Acrylates/C10-30 Akyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum).

* Please review the disclaimer below.