68479-909 NDC - INVISIBLE PHYSICAL DEFENSE SPF 30 ()

Drug Information

  • Product NDC: 68479-909
  • Proprietary Name: Invisible Physical Defense 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:3/5/2020

Package Information

No. Package Code Package Description Billing Unit
168479-909-00177 mL in 1 TUBE (68479-909-00)
268479-909-011 TUBE in 1 CARTON (68479-909-01) / 7 mL in 1 TUBE
368479-909-0250 mL in 1 TUBE (68479-909-02)
468479-909-04177 mL in 1 TUBE (68479-909-04)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68479-909Name of Company corresponding to the labeler code segment of the Product NDC.
PROPRIETARY NAMEInvisible Physical Defense SPF 30Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
START MARKETING DATE3/5/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERpart352This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEDermalogica, Inc. 

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

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