NDC 11489-060 Botanics Complexion Refining Day Moisture Sunscreen Spf 12

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:
11489-060
Proprietary Name:
Botanics Complexion Refining Day Moisture Sunscreen Spf 12
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
11489
Start Marketing Date: [9]
01-27-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 11489-060?

The NDC code 11489-060 is assigned by the FDA to the product Botanics Complexion Refining Day Moisture Sunscreen Spf 12 which is product labeled by Bcm Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11489-060-01 1 tube in 1 carton / 75 ml 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 Botanics Complexion Refining Day Moisture Sunscreen Spf 12?

DirectionsMassage onto face and neck with gentle upward strokes.Apply evenly at least 15 minutes before sun exposure.Reapply as required.Not intended for children under the age of 12.Not intended for protection while sunbathing. DIRECTIONS: Massage onto face and neck using gentle upward strokes.MODE D'EMPLOI: Massez sur le visage et le cou en suivant des mouvements ascendants.

Which are Botanics Complexion Refining Day Moisture Sunscreen Spf 12 UNII Codes?

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

Which are Botanics Complexion Refining Day Moisture Sunscreen Spf 12 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".