Saniluxe Hand Sanitizer Alcohol Free
Benzalkonium Chloride
Celeste Industries Corporation
Human Otc Drug
NDC 71489-008Saniluxe Hand Sanitizer Alcohol Free also known as Benzalkonium Chloride is a human otc drug labeled by 'Celeste Industries Corporation'. National Drug Code (NDC) number for Saniluxe Hand Sanitizer Alcohol Free is 71489-008. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Saniluxe Hand Sanitizer Alcohol Free drug includes Benzalkonium Chloride - 1 mg/mL . The currest status of Saniluxe Hand Sanitizer Alcohol Free drug is Active.
Drug Information:
| Drug NDC: | 71489-008 |
| 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: | Saniluxe Hand Sanitizer Alcohol Free |
| 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: | Benzalkonium Chloride |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Celeste Industries Corporation |
| 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: | BENZALKONIUM CHLORIDE - 1 mg/mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | CUTANEOUS
|
| 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: | 19 Feb, 2019 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 21 Dec, 2025 |
| 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: | part333E |
| 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, 2023 |
| 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: | Celeste Industries Corporation
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1049228
|
| 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. |
| UNII: | F5UM2KM3W7
|
| 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 |
|---|
| 71489-008-01 | 284 mL in 1 BOTTLE, PUMP (71489-008-01) | 19 Feb, 2019 | N/A | No |
| 71489-008-02 | 177 mL in 1 BOTTLE (71489-008-02) | 25 Jun, 2020 | N/A | No |
| 71489-008-03 | 59 mL in 1 BOTTLE, PUMP (71489-008-03) | 25 Jun, 2020 | N/A | No |
| 71489-008-04 | 237 mL in 1 BOTTLE, PUMP (71489-008-04) | 25 Jun, 2020 | N/A | No |
| 71489-008-05 | 355 mL in 1 BOTTLE, PUMP (71489-008-05) | 25 Jun, 2020 | N/A | No |
| 71489-008-06 | 3785 mL in 1 BOTTLE (71489-008-06) | 25 Jun, 2020 | N/A | No |
| 71489-008-07 | 59 mL in 1 BOTTLE (71489-008-07) | 25 Jun, 2020 | N/A | No |
| 71489-008-08 | 177 mL in 1 BOTTLE, PUMP (71489-008-08) | 25 Jun, 2020 | N/A | No |
| 71489-008-09 | 237 mL in 1 BOTTLE (71489-008-09) | 25 Jun, 2020 | N/A | No |
| 71489-008-10 | 284 mL in 1 BOTTLE (71489-008-10) | 25 Jun, 2020 | N/A | No |
| 71489-008-11 | 355 mL in 1 BOTTLE (71489-008-11) | 25 Jun, 2020 | N/A | No |
| 71489-008-12 | 3785 mL in 1 BOTTLE, PUMP (71489-008-12) | 25 Jun, 2020 | N/A | No |
| 71489-008-13 | 946 mL in 1 BOTTLE (71489-008-13) | 30 Jun, 2020 | N/A | No |
| 71489-008-14 | 946 mL in 1 BOTTLE, PUMP (71489-008-14) | 30 Jun, 2020 | N/A | No |
| 71489-008-15 | 530 mL in 1 BOTTLE (71489-008-15) | 14 Oct, 2020 | N/A | No |
| 71489-008-16 | 530 mL in 1 BOTTLE, PUMP (71489-008-16) | 14 Oct, 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 antimicrobial
Product Elements:
Saniluxe hand sanitizer alcohol free benzalkonium chloride water triethylene glycol glycereth-26 cocamidopropyl propylene glycol-dimonium chloride phosphate hydroxyethyl cellulose (5000 mpa.s at 1%) dmdm hydantoin trolamine iodopropynyl butylcarbamate butylene glycol benzalkonium chloride benzalkonium
Indications and Usage:
Uses recommended for repeated use for hand sanitizing to decrease bacteria on the skin
Warnings:
Warnings for external use only. keep out of reach of children. when using this product avoid contact with eyes. in case of eye contact, flush eyes with water. stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. if swallowed, get medical help or contact a poison control center right away.
When Using:
When using this product avoid contact with eyes. in case of eye contact, flush eyes with water.
Dosage and Administration:
Directions pump a small amount of gel into palm of hand rub hands together briskly until dry rub thoroughly over all surfaces of both hands
Stop Use:
Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. if swallowed, get medical help or contact a poison control center right away.
Package Label Principal Display Panel:
Principal display panel - 284 ml bottle label saniluxe⢠hand sanitizer gel alcohol free requires no water or towels. apply small amount to hands and rub until dry. kills 99% of germs on contact caution: use on hands only. 284ml e principal display panel - 284 ml bottle label