NDC 61625-682 Piranha Brand Alcohol Free Foaming Instant Hand Sanitizer With Aloe And Vitamin E

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61625-682
Proprietary Name:
Piranha Brand Alcohol Free Foaming Instant Hand Sanitizer With Aloe And Vitamin E
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
61625
Start Marketing Date: [9]
05-17-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 61625-682?

The NDC code 61625-682 is assigned by the FDA to the product Piranha Brand Alcohol Free Foaming Instant Hand Sanitizer With Aloe And Vitamin E which is product labeled by Bio Shine, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61625-682-41 1000 ml in 1 bag . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Piranha Brand Alcohol Free Foaming Instant Hand Sanitizer With Aloe And Vitamin E?

Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.Avoid contact with eyes. If contact occurs, flush with water.Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.Keep out of reach of children. If swallowed, contact a physician or poison control center.

Which are Piranha Brand Alcohol Free Foaming Instant Hand Sanitizer With Aloe And Vitamin E UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Piranha Brand Alcohol Free Foaming Instant Hand Sanitizer With Aloe And Vitamin E Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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] 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".