82723-006 NDC - TATTOO ULTRA SUNSCREEN ()

Drug Information

  • Product NDC: 82723-006
  • Proprietary Name: TATTOO ULTRA SUNSCREEN
  • Non Proprietary Name:
  • Active Ingredient(s): 19.5 g/100g TITANIUM DIOXIDE; 24 g/100g ZINC OXIDE
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Aopline Health Industry Technology (Guangzhou) Co., Ltd.
Product Type:
FDA Application Number: M020
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:11/1/2023
End Marketing Date:12/6/2023

Package Information

No. Package Code Package Description Billing Unit
182723-006-016 g in 1 BOTTLE (82723-006-01)
282723-006-0190 mL in 1 BOX (82723-006-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC82723-006The 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 NAMETATTOO ULTRA SUNSCREENThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/1/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
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 NAMEAopline Health Industry Technology (Guangzhou) Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC82723-006The 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 NAMEAloha mineral block-BRUSH ON MINERAL Powder SUNSCREEN SPF50The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/21/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
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 NAMEAopline Health Industry Technology (Guangzhou) 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: 11/21/2025

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