NDC 74598-112 Hand Sanitizer 70 Percent

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:
74598-112
Proprietary Name:
Hand Sanitizer 70 Percent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sunshine Tape Products Llc
Labeler Code:
74598
Start Marketing Date: [9]
04-03-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 74598-112-11

Package Description: 3785 mL in 1 JUG

NDC Code 74598-112-12

Package Description: 59 mL in 1 BOTTLE

NDC Code 74598-112-14

Package Description: 118 mL in 1 BOTTLE

NDC Code 74598-112-16

Package Description: 476 mL in 1 BOTTLE

NDC Code 74598-112-18

Package Description: 237 mL in 1 BOTTLE

Product Details

What is NDC 74598-112?

The NDC code 74598-112 is assigned by the FDA to the product Hand Sanitizer 70 Percent which is product labeled by Sunshine Tape Products Llc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 74598-112-11 3785 ml in 1 jug , 74598-112-12 59 ml in 1 bottle , 74598-112-14 118 ml in 1 bottle , 74598-112-16 476 ml in 1 bottle , 74598-112-18 237 ml in 1 bottle . 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 Hand Sanitizer 70 Percent?

Dispense enough product onto hands and rub together quickly until dry. Children under 6 years of age, use only under adult supervision.

Which are Hand Sanitizer 70 Percent UNII Codes?

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

Which are Hand Sanitizer 70 Percent 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:

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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".