NDC 55560-0101 Andalou Bb Untinted With 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:
55560-0101
Proprietary Name:
Andalou Bb Untinted With Spf-30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Andalou Naturals
Labeler Code:
55560
Start Marketing Date: [9]
12-10-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 55560-0101-1

Package Description: 58 mL in 1 TUBE

Product Details

What is NDC 55560-0101?

The NDC code 55560-0101 is assigned by the FDA to the product Andalou Bb Untinted With Spf-30 which is product labeled by Andalou Naturals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55560-0101-1 58 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 Andalou Bb Untinted With Spf-30?

Daily, alone or under make-up.Apply liberally 15 minutes before sun exposure and as needed.Reapply at least every 2 hours.Use water resistant sunscreen if swimming or sweating.Sun 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, especially from 10am-2pm, wear long sleeve shirts, pants and sunglasses.Children under 6 months: ask a doctor.

Which are Andalou Bb Untinted With Spf-30 UNII Codes?

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

Which are Andalou Bb Untinted With 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".