NDC 76665-025 Fundamentals Handlotion

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:
76665-025
Proprietary Name:
Fundamentals Handlotion
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Clean Beauty Concepts
Labeler Code:
76665
Start Marketing Date: [9]
09-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76665-025-01

Package Description: 3785 mL in 1 BOTTLE, DISPENSING

NDC Code 76665-025-02

Package Description: 60 mL in 1 BOTTLE, DISPENSING

NDC Code 76665-025-08

Package Description: 236 mL in 1 BOTTLE, DISPENSING

NDC Code 76665-025-16

Package Description: 473 mL in 1 BOTTLE, DISPENSING

Product Details

What is NDC 76665-025?

The NDC code 76665-025 is assigned by the FDA to the product Fundamentals Handlotion which is product labeled by Clean Beauty Concepts. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 76665-025-01 3785 ml in 1 bottle, dispensing , 76665-025-02 60 ml in 1 bottle, dispensing , 76665-025-08 236 ml in 1 bottle, dispensing , 76665-025-16 473 ml in 1 bottle, dispensing . 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 Fundamentals Handlotion?

Dispense lotion onto hands and rub into skin until absorbedSupervise children under 6 years of age when using this product to avoid swallowing

Which are Fundamentals Handlotion UNII Codes?

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

Which are Fundamentals Handlotion 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:

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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".