83872-100 NDC - BULUBIU MINERAL SUNSCREEN ()

Drug Information

  • Product NDC: 83872-100
  • Proprietary Name: bulubiu mineral sunscreen
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Shenzhen XiaoMai Manufacturing Co., Ltd.
Product Type:
FDA Application Number: M020
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:4/10/2024
End Marketing Date:1/1/2025

Package Information

No. Package Code Package Description Billing Unit
183872-100-0150 g in 1 BOTTLE (83872-100-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC83872-100The 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 NAMEbulubiu mineral sunscreenIndicates 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.
START MARKETING DATE4/10/2024The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
END MARKETING DATE1/1/2025The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGThe translation of the dosage form Code submitted by the firm.
APPLICATION NUMBERM020The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAMEShenzhen XiaoMai Manufacturing 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