NDC 78370-101 Antibacterial Free Gel

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:
78370-101
Proprietary Name:
Antibacterial Free Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Guangzhou Xin Qi Cosmetics Co., Ltd.
Labeler Code:
78370
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 78370-101-01

Package Description: 60 mL in 1 BOTTLE

NDC Code 78370-101-02

Package Description: 80 mL in 1 BOTTLE

NDC Code 78370-101-03

Package Description: 100 mL in 1 BOTTLE

NDC Code 78370-101-04

Package Description: 200 mL in 1 BOTTLE

NDC Code 78370-101-05

Package Description: 250 mL in 1 BOTTLE

NDC Code 78370-101-06

Package Description: 300 mL in 1 BOTTLE

NDC Code 78370-101-07

Package Description: 500 mL in 1 BOTTLE

NDC Code 78370-101-08

Package Description: 1000 mL in 1 BOTTLE

NDC Code 78370-101-09

Package Description: 5000 mL in 1 BOTTLE

NDC Code 78370-101-10

Package Description: 10000 mL in 1 BOTTLE

NDC Code 78370-101-11

Package Description: 4000 mL in 1 BOTTLE

NDC Code 78370-101-12

Package Description: 2000 mL in 1 BOTTLE

NDC Code 78370-101-13

Package Description: 1500 mL in 1 BOTTLE

NDC Code 78370-101-14

Package Description: 236 mL in 1 BOTTLE

NDC Code 78370-101-15

Package Description: 240 mL in 1 BOTTLE

NDC Code 78370-101-16

Package Description: 30 mL in 1 BOTTLE

NDC Code 78370-101-17

Package Description: 3800 mL in 1 BOTTLE

NDC Code 78370-101-18

Package Description: 5 mL in 1 BOTTLE

NDC Code 78370-101-19

Package Description: 8 mL in 1 BOTTLE

NDC Code 78370-101-20

Package Description: 50 mL in 1 BOTTLE

NDC Code 78370-101-21

Package Description: 3 mL in 1 BOTTLE

Product Details

What is NDC 78370-101?

The NDC code 78370-101 is assigned by the FDA to the product Antibacterial Free Gel which is product labeled by Guangzhou Xin Qi Cosmetics Co., Ltd.. The product's dosage form is . The product is distributed in 21 packages with assigned NDC codes 78370-101-01 60 ml in 1 bottle , 78370-101-02 80 ml in 1 bottle , 78370-101-03 100 ml in 1 bottle , 78370-101-04 200 ml in 1 bottle , 78370-101-05 250 ml in 1 bottle , 78370-101-06 300 ml in 1 bottle , 78370-101-07 500 ml in 1 bottle , 78370-101-08 1000 ml in 1 bottle , 78370-101-09 5000 ml in 1 bottle , 78370-101-10 10000 ml in 1 bottle , 78370-101-11 4000 ml in 1 bottle , 78370-101-12 2000 ml in 1 bottle , 78370-101-13 1500 ml in 1 bottle , 78370-101-14 236 ml in 1 bottle , 78370-101-15 240 ml in 1 bottle , 78370-101-16 30 ml in 1 bottle , 78370-101-17 3800 ml in 1 bottle , 78370-101-18 5 ml in 1 bottle , 78370-101-19 8 ml in 1 bottle , 78370-101-20 50 ml in 1 bottle , 78370-101-21 3 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 Antibacterial Free Gel?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Antibacterial Free Gel UNII Codes?

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

Which are Antibacterial Free Gel 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 Antibacterial Free Gel?

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:

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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".