NDC 61995-2089 Alba Botanica Mineral Sunscreen Ff Spf30

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:
61995-2089
Proprietary Name:
Alba Botanica Mineral Sunscreen Ff Spf30
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]
01-02-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61995-2089-5

Package Description: 113 g in 1 TUBE

NDC Code 61995-2089-6

Package Description: 170 g in 1 TUBE

Product Details

What is NDC 61995-2089?

The NDC code 61995-2089 is assigned by the FDA to the product Alba Botanica Mineral Sunscreen Ff Spf30 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 61995-2089-5 113 g in 1 tube , 61995-2089-6 170 g 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 Alba Botanica Mineral Sunscreen Ff Spf30?

Helps prevent sunburns. If used as directed with other sun protection measures decreases the risk of skin cancer and skin aging caused by the sun. Sun Protection Measures: Spending time on the sun increases your risk of skin cancer and skin aging. To decrease the risk regulary use Broad Spectrum Sunscreen with SPF 15 or higher and other protective measures including: limit time in sun, especially from 10am to 2 pm, and wear long-sleeved shirts, pants, hats ans sunglasses.

Which are Alba Botanica Mineral Sunscreen Ff Spf30 UNII Codes?

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

Which are Alba Botanica Mineral Sunscreen Ff Spf30 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".