NDC 58443-0294 Black Girl Sunscreen Spf 50 Broad Spectrum

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:
58443-0294
Proprietary Name:
Black Girl Sunscreen Spf 50 Broad Spectrum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
58443
Start Marketing Date: [9]
04-29-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE TO OFF WHITE)

Code Structure Chart

Product Details

What is NDC 58443-0294?

The NDC code 58443-0294 is assigned by the FDA to the product Black Girl Sunscreen Spf 50 Broad Spectrum which is product labeled by Prime Enterprises Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58443-0294-3 89 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 Black Girl Sunscreen Spf 50 Broad Spectrum?

Apply liberally 15 minutes before sun exposurereapplyafter 80 minutes of swimming or sweatinginmediately after towel dryingat least every 2 hoursSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures, including: limit time in the sun, specially from 10 a.m. - 2 p.m.wear long-sleeve shirts, pants, hats & sunglasses.children under 6 months: Ask a doctor.

Which are Black Girl Sunscreen Spf 50 Broad Spectrum UNII Codes?

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

Which are Black Girl Sunscreen Spf 50 Broad Spectrum 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".