NDC 77337-070 Wise Hands Instant Hand Sanitizer

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:
77337-070
Proprietary Name:
Wise Hands Instant Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Medwise Overseas Private Limited
Labeler Code:
77337
Start Marketing Date: [9]
05-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 77337-070-01

Package Description: 30 mL in 1 BOTTLE

NDC Code 77337-070-02

Package Description: 59 mL in 1 BOTTLE

NDC Code 77337-070-03

Package Description: 89 mL in 1 BOTTLE

NDC Code 77337-070-04

Package Description: 118 mL in 1 BOTTLE

NDC Code 77337-070-05

Package Description: 148 mL in 1 BOTTLE

NDC Code 77337-070-06

Package Description: 177 mL in 1 BOTTLE

NDC Code 77337-070-07

Package Description: 207 mL in 1 BOTTLE

NDC Code 77337-070-08

Package Description: 237 mL in 1 BOTTLE

NDC Code 77337-070-09

Package Description: 266 mL in 1 BOTTLE

NDC Code 77337-070-10

Package Description: 296 mL in 1 BOTTLE

NDC Code 77337-070-11

Package Description: 325 mL in 1 BOTTLE

NDC Code 77337-070-12

Package Description: 354 mL in 1 BOTTLE

NDC Code 77337-070-13

Package Description: 384 mL in 1 BOTTLE

NDC Code 77337-070-14

Package Description: 414 mL in 1 BOTTLE

NDC Code 77337-070-15

Package Description: 444 mL in 1 BOTTLE

NDC Code 77337-070-16

Package Description: 473 mL in 1 BOTTLE

NDC Code 77337-070-17

Package Description: 503 mL in 1 BOTTLE

NDC Code 77337-070-34

Package Description: 1006 mL in 1 BOTTLE

NDC Code 77337-070-68

Package Description: 2011 mL in 1 BOTTLE

Product Details

What is NDC 77337-070?

The NDC code 77337-070 is assigned by the FDA to the product Wise Hands Instant Hand Sanitizer which is product labeled by Medwise Overseas Private Limited. The product's dosage form is . The product is distributed in 19 packages with assigned NDC codes 77337-070-01 30 ml in 1 bottle , 77337-070-02 59 ml in 1 bottle , 77337-070-03 89 ml in 1 bottle , 77337-070-04 118 ml in 1 bottle , 77337-070-05 148 ml in 1 bottle , 77337-070-06 177 ml in 1 bottle , 77337-070-07 207 ml in 1 bottle , 77337-070-08 237 ml in 1 bottle , 77337-070-09 266 ml in 1 bottle , 77337-070-10 296 ml in 1 bottle , 77337-070-11 325 ml in 1 bottle , 77337-070-12 354 ml in 1 bottle , 77337-070-13 384 ml in 1 bottle , 77337-070-14 414 ml in 1 bottle , 77337-070-15 444 ml in 1 bottle , 77337-070-16 473 ml in 1 bottle , 77337-070-17 503 ml in 1 bottle , 77337-070-34 1006 ml in 1 bottle , 77337-070-68 2011 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 Wise Hands Instant Hand Sanitizer?

This product is used as Antimicrobial

Which are Wise Hands Instant Hand Sanitizer UNII Codes?

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

Which are Wise Hands Instant Hand Sanitizer 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:

What is the NDC to RxNorm Crosswalk for Wise Hands Instant Hand Sanitizer?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* 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".