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NDC 36800-722 Ultimate Sheer Spf 55 Body

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 36800-722?
  4. Ultimate Sheer Spf 55 Body Uses
  5. Active Ingredients UNII Codes
  6. 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:
36800-722
Proprietary Name:
Ultimate Sheer Spf 55 Body
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Topco
Labeler Code:
36800
Product Label ID:
5a9c2f6d-1be4-47a8-9825-58f8a6b1ec0b
Start Marketing Date: [9]
12-13-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 36800-722?

The NDC code 36800-722 is assigned by the FDA to the product Ultimate Sheer Spf 55 Body which is product labeled by Topco. The product's dosage form is . The product is distributed in a single package with assigned NDC code 36800-722-04 141 g in 1 can . 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 Ultimate Sheer Spf 55 Body?

• spray liberally and spread evenly by hand 15 minutes before sun exposure• reapply: • after 80 minutes of swimming or sweating• immediately after towel drying • at least every 2 hours• hold container 4 to 6 inches from the skin to apply • do not spray directlyinto face. Spray on hands then apply to face. • do not apply in windyconditions • use in a well-ventilated area• Sun Protection Measures. Spending time in the sun increases your risk ofskin cancer and early skin aging. To decrease this risk, regularly use asunscreen with a broad spectrum SPF of 15 or higher and other sunprotection measures including: • limit time in the sun, especially from10 a.m. – 2 p.m. • wear long-sleeve shirts, pants, hats, and sunglasses• children under 6 months: Ask a doctor

Which are Ultimate Sheer Spf 55 Body UNII Codes?

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

Which are Ultimate Sheer Spf 55 Body 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".