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  2. Autumn Harp, Inc
  3. NDC Product Code: 51514-0218 Gap Favorite Lip Balm Pomegranate Spf 18

NDC 51514-0218 Gap Favorite Lip Balm Pomegranate Spf 18

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. Product Characteristics
    4. What is NDC 51514-0218?
    5. Gap Favorite Lip Balm Pomegranate Spf 18 Uses
    6. Active Ingredients UNII Codes
    7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51514-0218
Proprietary Name:
Gap Favorite Lip Balm Pomegranate Spf 18
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Autumn Harp, Inc
Labeler Code:
51514
Product Label ID:
01c0a87e-52a3-48ca-8a08-5ec489e2d6f3
Start Marketing Date: [9]
11-16-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
FRUIT (C73389)

Product Packages

NDC Code 51514-0218-1

Package Description: 4 g in 1 CONTAINER

Product Details

What is NDC 51514-0218?

The NDC code 51514-0218 is assigned by the FDA to the product Gap Favorite Lip Balm Pomegranate Spf 18 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 51514-0218-1 4 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 Gap Favorite Lip Balm Pomegranate Spf 18?

Apply liberally before sun exposure and as neededchildren under 6 months of age: ask doctor

Which are Gap Favorite Lip Balm Pomegranate Spf 18 UNII Codes?

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

Which are Gap Favorite Lip Balm Pomegranate Spf 18 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".