11559-932 NDC - RESILIENCE LIFT ()

Drug Information

  • Product NDC: 11559-932
  • Proprietary Name: RESILIENCE LIFT
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: ESTEE LAUDER INC
Product Type:
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:5/1/2008

Package Information

No. Package Code Package Description Billing Unit
111559-932-011 JAR in 1 CARTON (11559-932-01) / 50 mL in 1 JAR (11559-932-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC11559-932The 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 NAMERESILIENCE LIFTThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXEXTREME ULTRA FIRMING SPF 15This is the date that the labeler indicates was the start of its marketing of the drug product.
START MARKETING DATE5/1/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALThis 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.
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 NAMEESTEE LAUDER INCName of Company corresponding to the labeler code segment of the Product NDC.

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

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