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  4. NDC Product Code: 69291-0850 Newgel Plus Spf

NDC 69291-0850 Newgel Plus Spf

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69291-0850?
  4. Newgel Plus Spf 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:
69291-0850
Proprietary Name:
Newgel Plus Spf
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Newmedical Technology, Inc.
Labeler Code:
69291
Product Label ID:
051735b9-d24c-595d-e054-00144ff88e88
Start Marketing Date: [9]
08-01-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69291-0850-1

Package Description: 1 BOTTLE, PUMP in 1 CARTON / 15 g in 1 BOTTLE, PUMP (69291-0850-2)

Product Details

What is NDC 69291-0850?

The NDC code 69291-0850 is assigned by the FDA to the product Newgel Plus Spf which is product labeled by Newmedical Technology, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69291-0850-1 1 bottle, pump in 1 carton / 15 g in 1 bottle, pump (69291-0850-2). 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 Newgel Plus Spf?

This product is used as

Which are Newgel Plus Spf UNII Codes?

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

Which are Newgel Plus Spf 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:

  • DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
  • POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)

* Please review the disclaimer below.

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".