NDC 69711-902 Deserving Health Natural Sunblock

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:
69711-902
Proprietary Name:
Deserving Health Natural Sunblock
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Deserving Health International Corp.
Labeler Code:
69711
Start Marketing Date: [9]
02-21-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 69711-902-01

Package Description: 120 mL in 1 TUBE

NDC Code 69711-902-02

Package Description: 240 mL in 1 TUBE

Product Details

What is NDC 69711-902?

The NDC code 69711-902 is assigned by the FDA to the product Deserving Health Natural Sunblock which is product labeled by Deserving Health International Corp.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69711-902-01 120 ml in 1 tube , 69711-902-02 240 ml in 1 tube . 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 Deserving Health Natural Sunblock?

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 Deserving Health Natural Sunblock UNII Codes?

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

Which are Deserving Health Natural Sunblock 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".