New Life Moisturizing Hand Sanitizer
Ethanol
New Life Products, Inc.
Human Otc Drug
NDC 49681-100New Life Moisturizing Hand Sanitizer also known as Ethanol is a human otc drug labeled by 'New Life Products, Inc.'. National Drug Code (NDC) number for New Life Moisturizing Hand Sanitizer is 49681-100. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in New Life Moisturizing Hand Sanitizer drug includes Alcohol - 70 mL/100mL . The currest status of New Life Moisturizing Hand Sanitizer drug is Active.
Drug Information:
| Drug NDC: | 49681-100 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | New Life Moisturizing Hand Sanitizer |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Ethanol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | New Life Products, Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Gel |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | ALCOHOL - 70 mL/100mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 27 Mar, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 05 May, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | part333A |
| 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. |
| Listing Expiration Date: | 31 Dec, 2024 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | New Life Products, Inc.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 581662
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 0743690091292
0743690091254
|
| UPC stands for Universal Product Code. |
| UNII: | 3K9958V90M
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 49681-100-01 | 30 mL in 1 BOTTLE, PLASTIC (49681-100-01) | 27 Mar, 2020 | N/A | No |
| 49681-100-02 | 60 mL in 1 BOTTLE, PLASTIC (49681-100-02) | 27 Mar, 2020 | N/A | No |
| 49681-100-04 | 3785 mL in 1 BOTTLE, PLASTIC (49681-100-04) | 26 Aug, 2020 | N/A | No |
| 49681-100-05 | 4.44 mL in 1 POUCH (49681-100-05) | 27 Mar, 2020 | N/A | No |
| 49681-100-10 | 59 mL in 1 TUBE (49681-100-10) | 27 Mar, 2020 | N/A | No |
| 49681-100-11 | 331 mL in 1 BOTTLE, PLASTIC (49681-100-11) | 27 Mar, 2020 | N/A | No |
| 49681-100-14 | 420 mL in 1 BOTTLE, PLASTIC (49681-100-14) | 27 Mar, 2020 | N/A | No |
| 49681-100-16 | 473 mL in 1 BOTTLE, PLASTIC (49681-100-16) | 27 Mar, 2020 | N/A | No |
| 49681-100-20 | 52 mL in 1 BOTTLE, PLASTIC (49681-100-20) | 27 Mar, 2020 | N/A | No |
| 49681-100-29 | 858 mL in 1 BOTTLE, PLASTIC (49681-100-29) | 27 Mar, 2020 | N/A | No |
| 49681-100-32 | 946 mL in 1 BOTTLE, PLASTIC (49681-100-32) | 27 Mar, 2020 | N/A | No |
| 49681-100-40 | 112 mL in 1 BOTTLE, PLASTIC (49681-100-40) | 27 Mar, 2020 | N/A | No |
| 49681-100-80 | 228 mL in 1 BOTTLE, PLASTIC (49681-100-80) | 27 Mar, 2020 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose antiseptic
Product Elements:
New life moisturizing hand sanitizer ethanol alcohol alcohol water polysorbate 20 isopropyl alcohol .alpha.-tocopherol acetate panthenol methyl gluceth-20 carbomer interpolymer type a (allyl sucrose crosslinked) aminomethylpropanol
Indications and Usage:
Uses ⢠hand sanitizer to decrease bacteria on skin ⢠recommended for repeated use
Warnings:
Warnings ⢠for external use only flammable. 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. keep out of reach of children.
Dosage and 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.
Package Label Principal Display Panel:
Packaging life1 life2 life3 life4 image