NDC 61995-2394 Alba Lip Care Sunblock Spf 25

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:
61995-2394
Proprietary Name:
Alba Lip Care Sunblock Spf 25
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]
10-27-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61995-2394-1

Package Description: 1 CANISTER in 1 CARTON / 4.2 g in 1 CANISTER

Product Details

What is NDC 61995-2394?

The NDC code 61995-2394 is assigned by the FDA to the product Alba Lip Care Sunblock Spf 25 which is product labeled by The Hain Celestial Group, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61995-2394-1 1 canister in 1 carton / 4.2 g in 1 canister. 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 Lip Care Sunblock Spf 25?

                             USES    Helps prevent sunburns    Higher SPF gives more sunburn protection    Apply liberally as needed 15 to 20 minutes before sun exposure     Reapply as needed or after swimming, perspiring or towel drying     Children under 6 months of age: ask doctor

Which are Alba Lip Care Sunblock Spf 25 UNII Codes?

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

* Please review the disclaimer below.

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".