NDC 80613-000-00 Action Instant Hand Sanitizer

Package Information

What is NDC 80613-000-00?

The NDC Code 80613-000-00 is assigned to a package of 500 ml in 1 bottle of Action Instant Hand Sanitizer, labeled by Maestro Laboratories Sdn. Bhd.. The product's dosage form is and is administered via form. The following table has all the important details about this NDC code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

Field Name Field Value
NDC Code 80613-000-00
Package Description 500 mL in 1 BOTTLE
Product Code 80613-000
Proprietary Name 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.		 Action Instant Hand Sanitizer
Usage Information Product Usage Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.		 This product is used as Antimicrobial. Hand sanitizer helps to reduce bacteria on the skin that could cause diseaseRecommended for repeated use
11-Digit NDC Billing Format NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.		 80613000000
NDC to RxNorm Crosswalk
  • RxCUI: 1305100 - ethanol 75 % Topical Gel
  • RxCUI: 1305100 - ethanol 0.75 ML/ML Topical Gel
    • Labeler Name Maestro Laboratories Sdn. Bhd.
    Sample Package Sample Package?
    This field Indicates whether this package is a sample packaging or not.    		 No
    Start Marketing Date What is the Start Marketing Date?
    This is the date that the labeler indicates was the start of its marketing of the drug product.    		 10-01-2019
    Listing Expiration Date 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.    		 12-31-2021
    Exclude Flag 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".     		I
    NDC Code Structure
    This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

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