68479-805 NDC - PRISMA PROTECT SPF 30 ()

Drug Information

  • Product NDC: 68479-805
  • Proprietary Name: Prisma Protect SPF 30
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Dermalogica, Inc.
Product Type:
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:3/7/2019

Package Information

No. Package Code Package Description Billing Unit
168479-805-002 mL in 1 POUCH (68479-805-00)
268479-805-0112 mL in 1 TUBE (68479-805-01)
368479-805-0250 mL in 1 TUBE (68479-805-02)
468479-805-041 TUBE in 1 CARTON (68479-805-04) / 177 mL in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC68479-805The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEPrisma Protect SPF 30Indicates 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.
START MARKETING DATE3/7/2019The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
APPLICATION NUMBERpart352The translation of the dosage form Code submitted by the firm.
LABELER NAMEDermalogica, Inc.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.

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This page was last updated on: 12/6/2025