71596-013 NDC - WAKEMAKE LIP COASTER M08 SALMON TWIST ()

Drug Information

  • Product NDC: 71596-013
  • Proprietary Name: WAKEMAKE LIP COASTER M08 SALMON TWIST
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: CJ OliveNetworks Co., Ltd.
Product Type:
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:7/1/2017
End Marketing Date:12/1/2018

Package Information

No. Package Code Package Description Billing Unit
171596-013-021 CONTAINER in 1 CARTON (71596-013-02) / 4.5 g in 1 CONTAINER (71596-013-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71596-013The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
PROPRIETARY NAMEWAKEMAKE LIP COASTER M08 SALMON TWISTThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE7/1/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE12/1/2018Product 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.
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 NUMBERpart347This 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 NAMECJ OliveNetworks Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.

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

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