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  4. NDC Product Code: 55777-0200 Natural For Family Spf 30

NDC 55777-0200 Natural For Family Spf 30

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55777-0200?
  4. Natural For Family Spf 30 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:
55777-0200
Proprietary Name:
Natural For Family Spf 30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sun Research Llc
Labeler Code:
55777
Product Label ID:
91035a82-ba8d-4b5f-ad4e-8a42e527f2e0
Start Marketing Date: [9]
01-01-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 55777-0200?

The NDC code 55777-0200 is assigned by the FDA to the product Natural For Family Spf 30 which is product labeled by Sun Research Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55777-0200-1 155 g 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 Natural For Family Spf 30?

Apply liberally 15 minutes before sun exposureReapply:After 80 minutes of swimming or sweatingImmediately after towel dryingAt least every 2 hoursChildren under 6 months: Ask a doctor

Which are Natural For Family Spf 30 UNII Codes?

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

Which are Natural For Family Spf 30 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".