NDC 12027-102 Wet N Wild Ultimate Match

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:
12027-102
Proprietary Name:
Wet N Wild Ultimate Match
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Markwins Beauty Products, Inc
Labeler Code:
12027
Start Marketing Date: [9]
12-01-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 12027-102-29

Package Description: 29.6 mL in 1 BOTTLE, GLASS

Product Details

What is NDC 12027-102?

The NDC code 12027-102 is assigned by the FDA to the product Wet N Wild Ultimate Match which is product labeled by Markwins Beauty Products, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 12027-102-29 29.6 ml in 1 bottle, glass . 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 Wet N Wild Ultimate Match?

Use• Helps prevent sunburn Directions • apply liberally 15 minutes before sun exposure • reapply at least every 2 hours • use a water resistant sunscreen if swimming or sweating • children under 6 months: Ask a doctor

Which are Wet N Wild Ultimate Match UNII Codes?

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

Which are Wet N Wild Ultimate Match 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".