64942-1326 NDC - DEGREE ()

Drug Information

  • Product NDC: 64942-1326
  • Proprietary Name: Degree
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Conopco Inc. d/b/a Unilever
Product Type:
FDA Application Number: part350
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:12/15/2013

Package Information

No. Package Code Package Description Billing Unit
164942-1326-174 g in 1 CONTAINER (64942-1326-1)
264942-1326-245 g in 1 CONTAINER (64942-1326-2)
364942-1326-314 g in 1 CONTAINER (64942-1326-3)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64942-1326The 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 NAMEDegreeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXMotion Sense Berry Cool Antiperspirant and DeodorantThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
START MARKETING DATE12/15/2013The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALThe translation of the route code submitted by the firm, indicating route of administration.
APPLICATION NUMBERpart350This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEConopco Inc. d/b/a UnileverProduct 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.

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This page was last updated on: 11/21/2025