NDC 69291-0850 Newgel Plus Spf

  1. Labeler Index
  2. Newmedical Technology, Inc.
  3. NDC: 69291-0850 Newgel Plus Spf

NDC Product Code 69291-0850

NDC CODE: 69291-0850

Proprietary Name: Newgel Plus Spf What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 69291 - Newmedical Technology, Inc.

NDC 69291-0850-1

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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Newgel Plus Spf with NDC 69291-0850 is a product labeled by Newmedical Technology, Inc.. The generic name of Newgel Plus Spf is . The product's dosage form is and is administered via form.

Labeler Name: Newmedical Technology, Inc.

Inactive Ingredient(s)

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

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Newmedical Technology, Inc.
Labeler Code: 69291
Start Marketing Date: 08-01-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2018 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.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

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Newgel Plus Spf Product Label Images