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  4. NDC Product Code: 71466-001 Bambo Nature Sunny Day

NDC 71466-001 Bambo Nature Sunny Day

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71466-001?
  4. Bambo Nature Sunny Day Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71466-001
Proprietary Name:
Bambo Nature Sunny Day
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Abena North America, Inc.
Labeler Code:
71466
Product Label ID:
5161c51f-ea23-1e7f-e054-00144ff8d46c
Start Marketing Date: [9]
06-01-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71466-001-01

Package Description: 150 g in 1 BOTTLE

NDC Code 71466-001-02

Package Description: 30 g in 1 BOTTLE

Product Details

What is NDC 71466-001?

The NDC code 71466-001 is assigned by the FDA to the product Bambo Nature Sunny Day which is product labeled by Abena North America, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 71466-001-01 150 g in 1 bottle , 71466-001-02 30 g 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 Bambo Nature Sunny Day?

Uses• helps prevent sunburn • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Which are Bambo Nature Sunny Day UNII Codes?

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

Which are Bambo Nature Sunny Day 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".