NDC 80110-015 Ethy Alcohol Wipes

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:
80110-015
Proprietary Name:
Ethy Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Anhui Germaphob Daily Commodity Co., Ltd.
Labeler Code:
80110
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 80110-015-01

Package Description: 1 CLOTH in 1 BAG

NDC Code 80110-015-02

Package Description: 10 CLOTH in 1 BAG

NDC Code 80110-015-03

Package Description: 20 CLOTH in 1 BAG

NDC Code 80110-015-04

Package Description: 40 CLOTH in 1 BAG

NDC Code 80110-015-05

Package Description: 50 CLOTH in 1 BAG

NDC Code 80110-015-06

Package Description: 80 CLOTH in 1 BAG

NDC Code 80110-015-07

Package Description: 100 CLOTH in 1 BAG

NDC Code 80110-015-08

Package Description: 120 CLOTH in 1 BAG

NDC Code 80110-015-09

Package Description: 40 CLOTH in 1 DRUM

NDC Code 80110-015-10

Package Description: 60 CLOTH in 1 DRUM

NDC Code 80110-015-11

Package Description: 80 CLOTH in 1 DRUM

NDC Code 80110-015-12

Package Description: 100 CLOTH in 1 DRUM

NDC Code 80110-015-13

Package Description: 120 CLOTH in 1 DRUM

NDC Code 80110-015-14

Package Description: 160 CLOTH in 1 DRUM

NDC Code 80110-015-15

Package Description: 200 CLOTH in 1 DRUM

NDC Code 80110-015-16

Package Description: 250 CLOTH in 1 DRUM

NDC Code 80110-015-17

Package Description: 260 CLOTH in 1 DRUM

NDC Code 80110-015-18

Package Description: 400 CLOTH in 1 DRUM

NDC Code 80110-015-19

Package Description: 600 CLOTH in 1 DRUM

NDC Code 80110-015-20

Package Description: 800 CLOTH in 1 DRUM

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".