NDC 62111-0211 Moisturizing Lip Balmspf30

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:
62111-0211
Proprietary Name:
Moisturizing Lip Balmspf30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Akg Innovations Llc
Labeler Code:
62111
Start Marketing Date: [9]
02-06-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62111-0211-3

Package Description: 1 TUBE in 1 BOX / 4.3 g in 1 TUBE

Product Details

What is NDC 62111-0211?

The NDC code 62111-0211 is assigned by the FDA to the product Moisturizing Lip Balmspf30 which is product labeled by Akg Innovations Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62111-0211-3 1 tube in 1 box / 4.3 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 Moisturizing Lip Balmspf30?

■Apply liberally and evenly 15 minutes before sun exposure.■Reapply at least every two hours.■Sun Protection Measures: Spending time in the sun increasesyour risk of skin cancer and early skin aging. To decrease this risk,regularly use a sunscreen with a Broad Spectrum SPF value of 15or higher and other sun protection measures including:• limit time in the sun, especially from 10 AM – 2 PM• wear long sleeve shirts, pants, hats, and sunglasses

Which are Moisturizing Lip Balmspf30 UNII Codes?

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

Which are Moisturizing Lip Balmspf30 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".