NDC 73006-201 Only For - 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:
73006-201
Proprietary Name:
Only For - Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
O4 Global Trading Usa, Llc
Labeler Code:
73006
Start Marketing Date: [9]
06-23-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 73006-201-50

Package Description: 50 CLOTH in 1 PACKAGE

NDC Code 73006-201-51

Package Description: 100 CLOTH in 1 CANISTER

NDC Code 73006-201-52

Package Description: 50 CLOTH in 1 BAG

NDC Code 73006-201-53

Package Description: 50 CLOTH in 1 CANISTER

Product Details

What is NDC 73006-201?

The NDC code 73006-201 is assigned by the FDA to the product Only For - Wipes which is product labeled by O4 Global Trading Usa, Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 73006-201-50 50 cloth in 1 package , 73006-201-51 100 cloth in 1 canister , 73006-201-52 50 cloth in 1 bag , 73006-201-53 50 cloth in 1 canister . 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 Only For - Wipes?

• To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, and feed through dispenser hole in cover.• Use entire wipe to thoroughly wipe hands, fingers and wrists.• To sanitize, use multiple wipes.• Discard after single use.

Which are Only For - Wipes UNII Codes?

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

Which are Only For - Wipes 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".