NDC 72525-003 Mineral Sunscreen Broad Spectrum 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:
72525-003
Proprietary Name:
Mineral Sunscreen Broad Spectrum Spf 30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
72525
Start Marketing Date: [9]
11-20-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 72525-003?

The NDC code 72525-003 is assigned by the FDA to the product Mineral Sunscreen Broad Spectrum Spf 30 which is product labeled by Recovery Care Products, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72525-003-01 14 g 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 Mineral Sunscreen Broad Spectrum Spf 30?

PLEASE ADHERE TO YOUR PHYSICIAN'S PROTOCOL FOR THIS PRODUCT*WOULD MUST BE FULLY CLOSED AND NO LONGER SCABBEDGENTLY GLIDE OVER SCAR 15 MINUTES PRIOR TO SUN EXPOSUREREAPPLY: AFTER 80 MINUTES OF SWIMMING OR SWEATING, IMMEDIATELY AFTER TOWEL DRYING, EVERY TWO HOURSCHILDREN UNDER 6 MONTHS: CONSULT YOUR PHYSICIANFOR OPTIMAL RESULTS, USE IN CONJUNCTION WITH RCP SCAR MANAGEMENT**FOR MORE INFORMATION ON PROTOCOLS VISIT WWW.RCPCARE.COM/RECOVERYRESOURCES

Which are Mineral Sunscreen Broad Spectrum Spf 30 UNII Codes?

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

Which are Mineral Sunscreen Broad Spectrum 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".