NDC 77965-001 Greenberry

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 77965-001?
    4. Greenberry Uses
    5. Active Ingredients UNII Codes
    6. Inactive Ingredients UNII Codes
    7. NDC to RxNorm Crosswalk

Product Information

NDC Product Code77965-001
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Greenberry
NDC Directory StatusINACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Greenberry Eco Group Llc
Labeler Code77965
SPL SET ID:013fd60f-e7f0-4098-b2f8-9e75c7fcc765
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		06-10-2020
Listing Expiration Date 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.		12-31-2022
Exclude Flag 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". 		I
NDC Code Structure

Product Packages

NDC Code 77965-001-01

Package Description: 10 NOT APPLICABLE in 1 POUCH / 3.8 mL in 1 NOT APPLICABLE

NDC Code 77965-001-02

Package Description: 72 NOT APPLICABLE in 1 CANISTER / 3.8 mL in 1 NOT APPLICABLE

NDC Code 77965-001-03

Package Description: 110 NOT APPLICABLE in 1 POUCH / 3.8 mL in 1 NOT APPLICABLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

What is NDC 77965-001?

The NDC code 77965-001 is assigned by the FDA to the product Greenberry which is product labeled by Greenberry Eco Group Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 77965-001-01 10 not applicable in 1 pouch / 3.8 ml in 1 not applicable, 77965-001-02 72 not applicable in 1 canister / 3.8 ml in 1 not applicable, 77965-001-03 110 not applicable in 1 pouch / 3.8 ml in 1 not applicable. 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 Greenberry?

This product is used as Antimicrobial agent. Decreases bacteria on skin.

Which are Greenberry UNII Codes?

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

Which are Greenberry 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 Greenberry?

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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