72839-411 NDC - ARUBA SUN MINERAL SUNSCREEN ()

Drug Information

  • Product NDC: 72839-411
  • Proprietary Name: Aruba Sun Mineral Sunscreen
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Derma Care Research Labs, LLC
Product Type:
FDA Application Number: M020
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:5/23/2023
End Marketing Date:1/2/2024

Package Information

No. Package Code Package Description Billing Unit
172839-411-0385 g in 1 TUBE (72839-411-03)
272839-411-1385 g in 1 TUBE (72839-411-13)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72839-411The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
PROPRIETARY NAMEAruba Sun Mineral SunscreenThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE5/23/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE1/2/2024This 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.
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 NAMEDerma Care Research Labs, LLCName 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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