NDC 41520-225 Instant Hand Sanitizer
NDC Product Code 41520-225
Proprietary Name: Instant 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 41520 - American Sales Company
- 41520-225 - Instant Hand Sanitizer
NDC 41520-225-15
Package Description: 443 mL in 1 BOTTLE
NDC Product Information
Instant Hand Sanitizer with NDC 41520-225 is a product labeled by American Sales Company. The generic name of Instant Hand Sanitizer is . The product's dosage form is and is administered via form.
Labeler Name: American Sales Company
Dosage Form: -
Product Type: 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.
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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- CARBOMER 934 (UNII: Z135WT9208)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: American Sales Company
Labeler Code: 41520
Start Marketing Date: 02-01-2013 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: 12-31-2019 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 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. Values = ‘Y’ or ‘N’.
* Please review the disclaimer below.
Instant Hand Sanitizer Product Label Images
Instant 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
- Uses
- Warnings
- When Using This Product
- Stop Using This Product And Ask Doctor If
- Keep Out Of Reach Of Children
- Directions
- Other Information
- Purpose
- Inactive Ingredients
Active Ingredient
ETHYL ALCOHOL 62%
Uses
TO HELP REDUCE BACTERIA ON THE SKIN.
Warnings
FOR EXTERNAL USE ONLY.
When Using This Product
- AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.
Stop Using This Product And Ask Doctor If
- IRRITATION OR RASH DEVELOPS AND LASTS.
Keep Out Of Reach Of Children
IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Directions
- APPLY A SMALL AMOUNT IN YOUR PALM AND RUB HANDS TOGETHER BRISKLY UNTIL DRY.CHILDREN UNDER 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.
Other Information
DO NOT STORE ABOVE 110OC (43 OC). MAY DISCOLOR CERTAIN FABRICS OR SURFACES.
Purpose
ANTISEPTIC
Inactive Ingredients
WATER, GLYCERIN, ISOPROPYL MYRISTATE, PROPYLENE GLYCOL, TOCOPHERYL ACETATE, AMINOMETHYL PROPANOL, CARBOMER, FRAGRANCE.
* Please review the disclaimer below.