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  4. NDC Product Code: 82080-101 Sunscreen Sprays

NDC 82080-101 Sunscreen Sprays

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82080-101?
  4. Sunscreen Sprays 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:
82080-101
Proprietary Name:
Sunscreen Sprays
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Headblock Llc
Labeler Code:
82080
Product Label ID:
c61c3a8f-eafd-3110-e053-2995a90a05c6
Start Marketing Date: [9]
07-02-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 82080-101?

The NDC code 82080-101 is assigned by the FDA to the product Sunscreen Sprays which is product labeled by Headblock Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82080-101-01 141 g in 1 bottle . 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 Sprays?

Shake well before use. Apply liberally 15 minutes before sun exposure and rub into skin. Hold container 4 to 6 inches from the skin to apply. Do not spray directly into face. Spray on hands then apply to face. Do not apply in windy conditions. Use in well-ventilated area. Reapply: After 80 minutes of swimming or sweating, immediately after towel drying, or at least every 2 hours. Children under 6 months: Ask a doctor. Other Information: protect this product from excessive heat and direct sun; may stain some fabrics.

Which are Sunscreen Sprays UNII Codes?

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

Which are Sunscreen Sprays 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".