NDC 69711-370 Lunchboxwax Body Spf 30

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:
69711-370
Proprietary Name:
Lunchboxwax Body Spf 30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Derma Soleil
Labeler Code:
69711
Start Marketing Date: [9]
09-10-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69711-370-01

Package Description: 100 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 69711-370?

The NDC code 69711-370 is assigned by the FDA to the product Lunchboxwax Body Spf 30 which is product labeled by Derma Soleil. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69711-370-01 100 ml in 1 bottle, plastic . 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 Lunchboxwax Body Spf 30?

The sun may cause sunburn, premature aging of the skin and skin cancer. Avoiding the sun, wearing protective clothing and regular use of sunscreens over the years reduces the chance of these harmful effects.Helps prevent sunburnIf used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by sun The sun may cause sunburn, premature aging of the skin and skin cancer. Avoiding the sun, wearing protective clothing and regular use of sunscreens over the years reduces the chance of these harmful effects. Users: Helps pprevent sunburn if used as directed with other sun protection measures. Decreases the risk of skin cancer and early skin aging cause by the sun.

Which are Lunchboxwax Body Spf 30 UNII Codes?

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

Which are Lunchboxwax Body Spf 30 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:

* Please review the disclaimer below.

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".