NDC 69291-0850 Newgel Plus Spf
NDC Product 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.
- 69291-0850 - Newgel Plus Spf
NDC 69291-0850-1
Package Description: 1 BOTTLE, PUMP in 1 CARTON > 15 g in 1 BOTTLE, PUMP (69291-0850-2)
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.
Dosage Form: -
Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
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 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. Values = ‘Y’ or ‘N’.
* Please review the disclaimer below.
Newgel Plus Spf Product Label Images
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Inactive Ingredients - Inactive Ingredients Section
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Purpose Zinc Oxide 20% Sunscreen - OTC Purpose section
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Zinc Oxide 20% Sunscreen - OTC Active Ingredients Section
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OTC-Keep out of Reach of Children - OTC Keep out of Reach of Children section
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Package Label - Package Label
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Silagen Bottle Pump 69291-6215-2 - Silagen Bottle Pump 69291 6215 2
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Silagen Bottle - Silagen Bottle Pump 69291 6230 2
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Silagen Carton - Silagen Carton 69291 6215 1
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Silagen Carton - Silagen Carton 69291 6230 1
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Warnings - Warnings Section