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Data / Drug companies / L.S. Moore LLC

L.S. Moore LLC: 7 products in the FDA NDC directory, labeler code 85768

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

L.S. Moore LLC (labeler code 85768) lists 7 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 7 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on December 20, 2024.

The request: Watch L.S. Moore LLC (FDA labeler code 85768): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
85768
Products in commercial distribution
7
Packages
7
Finished drugs by generic name
2
Prescription products
0
Over the counter products
7
Started marketing in the last 12 months
0
Earliest marketing start
July 16, 2024
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs7100%

Products by type

TypeProductsShare
Over the counter drugs7100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Zinc oxide4595
Titanium dioxide, zinc oxide3255

Dosage forms

Dosage formProductsShare
Cream7100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Original Tint85768-203CreamOver the counter monograph drugsDecember 20, 2024
Original Tint85768-201CreamOver the counter monograph drugsDecember 20, 2024
Hint of Tint85768-204CreamOver the counter monograph drugsSeptember 6, 2024
Hint of Tint85768-204CreamOver the counter monograph drugsSeptember 5, 2024
Radiance85768-226CreamOver the counter monograph drugsJuly 16, 2024
Radiance85768-226CreamOver the counter monograph drugsJuly 16, 2024
Original Tint85768-203CreamOver the counter monograph drugsJuly 16, 2024

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.