NDC 61995-2037 Alba Body Daily Shade Spf15

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:
61995-2037
Proprietary Name:
Alba Body Daily Shade Spf15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Hain Celestial Group, Inc.
Labeler Code:
61995
Start Marketing Date: [9]
11-11-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61995-2037-8

Package Description: 340 g in 1 BOTTLE

NDC Code 61995-2037-9

Package Description: 907 g in 1 BOTTLE

Product Details

What is NDC 61995-2037?

The NDC code 61995-2037 is assigned by the FDA to the product Alba Body Daily Shade Spf15 which is product labeled by The Hain Celestial Group, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 61995-2037-8 340 g in 1 bottle , 61995-2037-9 907 g in 1 bottle . 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 Alba Body Daily Shade Spf15?

Helps prevents sunburns. If uses as directed with other sun protection measures, decreases risk of skin cancer and early skin aging caused by sun exposure. Skin Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use sunscreen with Broad Spectrum SPF 15 or higher and other protective measures including: limit time in sun, especially from10am to 2pm, and wear long sleeved shirts, pants, hats and sunglases.

Which are Alba Body Daily Shade Spf15 UNII Codes?

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

Which are Alba Body Daily Shade Spf15 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".