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  4. NDC Product Code: 51401-030 Skin Strong - Skin Equipment Spf 30 Sunscreen

NDC 51401-030 Skin Strong - Skin Equipment Spf 30 Sunscreen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51401-030?
  4. Skin Strong - Skin Equipment Spf 30 Sunscreen 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:
51401-030
Proprietary Name:
Skin Strong - Skin Equipment Spf 30 Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
True Balance Athletics Llc
Labeler Code:
51401
Product Label ID:
683d6fd0-ea36-4fdf-932c-8c44bf80ab2d
Start Marketing Date: [9]
08-30-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 51401-030?

The NDC code 51401-030 is assigned by the FDA to the product Skin Strong - Skin Equipment Spf 30 Sunscreen which is product labeled by True Balance Athletics Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51401-030-01 118 ml in 1 bottle, pump . 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 Skin Strong - Skin Equipment Spf 30 Sunscreen?

APPLY LIBERALLY 20 MINUTES BEFORE SUN EXPOSURE AND AS NEEDEDFOR CHILDREN UNDER 6 MONTHS OF AGE, ASK A DOCTOR

Which are Skin Strong - Skin Equipment Spf 30 Sunscreen UNII Codes?

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

Which are Skin Strong - Skin Equipment Spf 30 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".