NDC 51514-0305 Alba Terratint Blaze Spf 15 Lip Balm

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:
51514-0305
Proprietary Name:
Alba Terratint Blaze Spf 15 Lip Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Autumn Harp, Inc.
Labeler Code:
51514
Start Marketing Date: [9]
08-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327)
Flavor(s):
PEPPERMINT (C73408)

Product Packages

NDC Code 51514-0305-1

Package Description: 4.2 g in 1 CONTAINER

Product Details

What is NDC 51514-0305?

The NDC code 51514-0305 is assigned by the FDA to the product Alba Terratint Blaze Spf 15 Lip Balm which is product labeled by Autumn Harp, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51514-0305-1 4.2 g in 1 container . 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 Terratint Blaze Spf 15 Lip Balm?

Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours. Children under 6 months: ask a doctor. Skin Protection Measures: Spending time in sun increases risk of skin cancer and early skin aging. To decrease risk, use sunscreen with Broad Spectrum SPF 15 or higher, limit time in sun, especially 10am-2pm, and wear hats and sunglasses.

Which are Alba Terratint Blaze Spf 15 Lip Balm UNII Codes?

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

Which are Alba Terratint Blaze Spf 15 Lip Balm 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".