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  4. NDC Product Code: 31190-330 Spf 30 Sunscreen

NDC 31190-330 Spf 30 Sunscreen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 31190-330?
  5. Spf 30 Sunscreen Uses
  6. Active Ingredients UNII Codes
  7. 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:
31190-330
Proprietary Name:
Spf 30 Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shanghai Kejing Cleaning Products Co., Ltd.
Labeler Code:
31190
Product Label ID:
ffec35ba-1267-461f-bfcd-25ed28482ada
Start Marketing Date: [9]
06-25-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
VANILLA (C73421)

Product Packages

NDC Code 31190-330-01

Package Description: 30 g in 1 BOTTLE

NDC Code 31190-330-02

Package Description: 60 g in 1 PACKAGE

Product Details

What is NDC 31190-330?

The NDC code 31190-330 is assigned by the FDA to the product Spf 30 Sunscreen which is product labeled by Shanghai Kejing Cleaning Products Co., Ltd.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 31190-330-01 30 g in 1 bottle , 31190-330-02 60 g in 1 package . 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 Spf 30 Sunscreen?

Uses: Helps prevent sunburn

Which are Spf 30 Sunscreen UNII Codes?

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

Which are Spf 30 Sunscreen 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".