NDC 69424-580 Leaders Sunbuddy Daily Moisture Sunscreen

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:
69424-580
Proprietary Name:
Leaders Sunbuddy Daily Moisture Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Leaders Cosmetics Co.,ltd.
Labeler Code:
69424
Start Marketing Date: [9]
02-10-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69424-580-02

Package Description: 1 TUBE in 1 CARTON / 70 mL in 1 TUBE (69424-580-01)

Product Details

What is NDC 69424-580?

The NDC code 69424-580 is assigned by the FDA to the product Leaders Sunbuddy Daily Moisture Sunscreen which is product labeled by Leaders Cosmetics Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69424-580-02 1 tube in 1 carton / 70 ml in 1 tube (69424-580-01). 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 Leaders Sunbuddy Daily Moisture Sunscreen?

Directions: Take an appropriate amount and apply thinly to the face and neck which is likely to be exposed to UV rays at the final stage of skin care. Finish by tapping lightly. Apply liberally 15 min before sun exposure. Reapply after 40min of swimming or sweating.

Which are Leaders Sunbuddy Daily Moisture Sunscreen UNII Codes?

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

Which are Leaders Sunbuddy Daily Moisture Sunscreen 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".