72220-001 NDC - MDP HYALURONIC ACID UV CLEAR SUNSCREEN SPF 55 ()

Drug Information

  • Product NDC: 72220-001
  • Proprietary Name: MDP Hyaluronic acid UV clear sunscreen SPF 55
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: SKINIDEA CO., LTD
Product Type:
FDA Application Number: M020
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:8/1/2024
End Marketing Date:10/30/2024

Package Information

No. Package Code Package Description Billing Unit
172220-001-011 TUBE in 1 CARTON (72220-001-01) / 40 mL in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC72220-001An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
PROPRIETARY NAMEMDP Hyaluronic acid UV clear sunscreen SPF 55 
START MARKETING DATE8/1/2024 
END MARKETING DATE10/30/2024 
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBERM020This 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 NAMESKINIDEA CO., LTDName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/19/2025

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