71252-110 NDC - QUEENS ROSE ROSE SKIN PERFECTION BB (TITANIUM DIOXIDE, ZINC OXIDE)

Drug Information

Product NDC: 71252-110

Proprietary Name: QUEENS ROSE ROSE SKIN PERFECTION BB

Non Proprietary Name: Titanium Dioxide, Zinc Oxide

Active Ingredient(s):
  • 6.69 g/50g TITANIUM DIOXIDE;
  • .72 g/50g ZINC OXIDE


Administration Route(s): TOPICAL

Dosage Form(s): CREAM

Labeler Information

Labeler Name: Cdpharmtec Co.,ltd
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/2/2017

Package Information

No. Package Code Package Description Billing Unit
171252-110-021 BOTTLE, PUMP in 1 CARTON (71252-110-02) > 50 g in 1 BOTTLE, PUMP (71252-110-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71252-110The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEQUEENS ROSE ROSE SKIN PERFECTION BBThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMETitanium Dioxide, Zinc OxideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/2/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT 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 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 NAMECdpharmtec Co.,ltdName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMETITANIUM DIOXIDE; ZINC OXIDEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH6.69; .72 
ACTIVE INGRED UNITg/50g; g/50g 

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This page was last updated on: 7/15/2019