Instant Hand Sanitizer
Ethyl Alcohol
Hillyard Gmp
Human Otc Drug
NDC 76402-422Instant Hand Sanitizer also known as Ethyl Alcohol is a human otc drug labeled by 'Hillyard Gmp'. National Drug Code (NDC) number for Instant Hand Sanitizer is 76402-422. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Instant Hand Sanitizer drug includes Alcohol - 62 mL/100mL . The currest status of Instant Hand Sanitizer drug is Active.
Drug Information:
| Drug NDC: | 76402-422 |
| 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: | Instant 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: | Ethyl Alcohol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Hillyard Gmp |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Spray |
| 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 - 62 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: | 16 Mar, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 06 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: | 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: | Hillyard GMP
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1020364
|
| 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: | 0780458011338
0780458011345
|
| 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 |
|---|
| 76402-422-02 | 3 BOTTLE, PLASTIC in 1 CARTON (76402-422-02) / 1000 mL in 1 BOTTLE, PLASTIC | 16 Mar, 2020 | N/A | No |
| 76402-422-03 | 4 BOTTLE, PLASTIC in 1 CARTON (76402-422-03) / 1000 mL in 1 BOTTLE, PLASTIC | 16 Mar, 2020 | N/A | No |
| 76402-422-31 | 6 BOTTLE, PUMP in 1 CARTON (76402-422-31) / 1000 mL in 1 BOTTLE, PUMP | 14 Aug, 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:
Instant hand sanitizer ethyl alcohol alcohol alcohol water peg-10 dimethicone (600 cst) glycerin citric acid monohydrate .alpha.-tocopherol aloe vera leaf
Indications and Usage:
Uses ⢠for hand sanitizing to decrease bacteria on the skin. ⢠recommended for repeated use.
Warnings:
Warnings ⢠for external use only flammable. keep away from fire or flame.
When Using:
When using this product avoid contact with eyes. in case of eye contact, flush eyes thoroughly with water.
Dosage and Administration:
Directions ⢠pump enough spray into palm of hand to cover both hands. ⢠rub thoroughly over all surfaces of both hands. ⢠rub hands together briskly until dry. ⢠children under 6 years of age should be supervised when using this product.
Stop Use:
Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.
Package Label Principal Display Panel:
Principal display panel â 1 liter (automatic dispenser) hillyard spray instant hand sanitizer hil0042202 affinity dispensing system place cartridge into dispenser, label facing back, and gently push pump into receiver until it clicks into place. to remove the cartridge and pump, rotate the green ring clockwise and pull the pump out. hillyard industries, inc. po box 909 st. joseph, mo 64502-0909 telephone: 816-233-1321 www.hillyard.com net contents: 33.8 fl oz or 1l peel here label image-01
Principal display panel â 1.00 liter (manual dispenser) hillyard spray instant hand sanitizer hil0042203 affinity dispensing system place cartridge into dispenser, label facing back, and gently push pump into receiver until it clicks into place. to remove the cartridge and pump, rotate the green ring clockwise and pull the pump out. hillyard industries, inc. po box 909 st. joseph, mo 64502-0909 telephone: 816-233-1321 www.hillyard.com net contents: 33.8 fl oz or 1l peel here label image-02
Principal display panel â 1.00 liter (manual dispensing pump) hillyard instant hand sanitizer spray kills 99.99% of illness causing germs moisturizes with aloe vitamin e and conditioners! 62% ethyl alcohol net contents: 1 liter or 0.264 gal hillyard industries, inc. po box 909 st. joseph, mo 64502-0909 telephone: 800-365-1555 www.hillyard.com label image-03