NDC 13630-0096 Prebel Nude Protect Spf 70 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:
13630-0096
Proprietary Name:
Prebel Nude Protect Spf 70 Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
13630
Start Marketing Date: [9]
03-07-2012
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Code Structure Chart

Product Details

What is NDC 13630-0096?

The NDC code 13630-0096 is assigned by the FDA to the product Prebel Nude Protect Spf 70 Sunscreen which is product labeled by Prime Packaging Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 13630-0096-4 177 ml in 1 can . 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 Prebel Nude Protect Spf 70 Sunscreen?

Apply generously to all areas 15 minutes before sun exposure. Spray into hands to apply to face, do not spray directly. Reapply as needed or after towel drying. Ask a doctor before use on children under 6 months of age. Limit sun exposure, wear protective clothing. This product may stain some fabrics.

Which are Prebel Nude Protect Spf 70 Sunscreen UNII Codes?

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

Which are Prebel Nude Protect Spf 70 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".