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Data / Drug companies / Sunjin Beauty Science Co., LTD.

Sunjin Beauty Science Co., LTD.: 28 products in the FDA NDC directory, labeler code 71028

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Sunjin Beauty Science Co., LTD. (labeler code 71028) lists 28 products in the FDA National Drug Code Directory. By type: 28 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on September 29, 2026.

The request: Watch Sunjin Beauty Science Co., LTD. (FDA labeler code 71028): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
71028
Products in commercial distribution
28
Packages
28
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
7
Earliest marketing start
July 3, 2019
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients28100%

Products by type

TypeProductsShare
Bulk ingredients28100%

Dosage forms

Dosage formProductsShare
Powder1967.9%
Liquid932.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Bis-ethylhexyloxyphenol methoxyphenyl triazine71028-3206PowderBulk ingredientsSeptember 29, 2026
Zinc oxide71028-3205PowderBulk ingredientsAugust 26, 2026
Zinc oxide71028-3204LiquidBulk ingredientsJuly 18, 2026
Butyl methoxydibenzoylmethane71028-3203PowderBulk ingredientsJune 8, 2026
Zinc oxide71028-2501PowderBulk ingredientsMay 18, 2026
Zinc oxide71028-3202LiquidBulk ingredientsJanuary 27, 2026
Zinc oxide71028-3201LiquidBulk ingredientsJanuary 27, 2026
Zinc oxide71028-2401PowderBulk ingredientsJuly 15, 2024
Zinc oxide71028-2310PowderBulk ingredientsAugust 27, 2023
Titanium dioxide71028-2304PowderBulk ingredientsAugust 18, 2023
Zinc oxide71028-2302LiquidBulk ingredientsAugust 18, 2023
Zinc oxide71028-2301LiquidBulk ingredientsAugust 18, 2023
Titanium dioxide71028-2214LiquidBulk ingredientsDecember 12, 2022
Titanium dioxide71028-2211LiquidBulk ingredientsDecember 12, 2022
Zinc oxide71028-2209LiquidBulk ingredientsDecember 12, 2022
Zinc oxide71028-2207LiquidBulk ingredientsDecember 12, 2022
Titanium dioxide71028-2206PowderBulk ingredientsDecember 12, 2022
Titanium dioxide71028-2205PowderBulk ingredientsDecember 12, 2022
Titanium dioxide71028-2204PowderBulk ingredientsDecember 12, 2022
Titanium dioxide71028-2203PowderBulk ingredientsDecember 12, 2022
Titanium dioxide71028-2202PowderBulk ingredientsDecember 12, 2022
Titanium dioxide71028-2201PowderBulk ingredientsDecember 12, 2022
Titanium dioxide71028-2001PowderBulk ingredientsSeptember 28, 2020
Titanium dioxide71028-1907PowderBulk ingredientsJanuary 20, 2020
Zinc oxide71028-1103PowderBulk ingredientsDecember 10, 2019

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.