NDC 71011-002 Sunscreen 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:
71011-002
Proprietary Name:
Sunscreen Lip Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
71011
Start Marketing Date: [9]
10-08-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 71011-002?

The NDC code 71011-002 is assigned by the FDA to the product Sunscreen Lip Balm which is product labeled by Ningbo Huize Commodity Co.,ltd.. The product's dosage form is . The product is distributed in 16 packages with assigned NDC codes 71011-002-01 10 g in 1 package , 71011-002-02 13 g in 1 package , 71011-002-03 14 g in 1 package , 71011-002-04 15 g in 1 package , 71011-002-05 16 g in 1 package , 71011-002-06 19 g in 1 package , 71011-002-07 20 g in 1 package , 71011-002-08 25 g in 1 package , 71011-002-09 30 g in 1 package , 71011-002-11 3 g in 1 package , 71011-002-12 4 g in 1 package , 71011-002-13 5 g in 1 package , 71011-002-14 6 g in 1 package , 71011-002-15 7 g in 1 package , 71011-002-16 8 g in 1 package , 71011-002-17 9 g in 1 package . 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 Sunscreen Lip Balm?

Directions ■Apply liberally 15 minutes before sun exposure ■after 80 minutes of swimming or sweating, immediately after towel drying. ■To decrease the risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher ■at least every 2 hours. ■ Spending time in the sun increases your risk of skin cancer and early skin aging

Which are Sunscreen Lip Balm UNII Codes?

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

Which are Sunscreen 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".