NDC 13630-0069 Ulta 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:
Proprietary Name:
Ulta Broad Spectrum Spf 30
Product Type: [3]
Labeler Name: [5]
Prime Packaging, Inc.
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Characteristics

YELLOW (C48330)

Product Packages

NDC Code 13630-0069-4

Package Description: 177 mL in 1 CAN

Product Details

What is NDC 13630-0069?

The NDC code 13630-0069 is assigned by the FDA to the product Ulta Broad Spectrum Spf 30 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 13630-0069-4 177 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 Ulta Broad Spectrum Spf 30?

Spray liberally and spread evenly by hand 15 minutes before sun exposurehold container 4 to 6 inches from the skin to applydo not spray directly into face. Spray on hands then apply to facedo not apply in windy conditionsuse in well-ventilated areasreapply:after 80 minutes of swimming or sweatingimmediately 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 broad spectrum SPF of 15 or higher and other sun protection measures including:limit time in the sun, especially from 10 a.m. – 2 p.m.wear long-sleeve shirts, pants, hats, and sunglassesChildren under 6 months: Ask a doctor

Which are Ulta Broad Spectrum Spf 30 UNII Codes?

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

Which are Ulta 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:

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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".