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Data / Drug companies / Supplement Clinic, LLC.

Supplement Clinic, LLC.: 7 products in the FDA NDC directory, labeler code 71781

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

Supplement Clinic, LLC. (labeler code 71781) lists 7 products in the FDA National Drug Code Directory. By type: 7 over the counter drugs. Its main marketing category is unapproved homeopathic products. The newest product started marketing on November 1, 2017.

The request: Watch Supplement Clinic, LLC. (FDA labeler code 71781): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
71781
Products in commercial distribution
7
Packages
7
Finished drugs by generic name
0
Prescription products
0
Over the counter products
7
Flagged as original packager
7 of 7 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
October 31, 2017
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Unapproved homeopathic products7100%

Products by type

TypeProductsShare
Over the counter drugs7100%

Dosage forms

Dosage formProductsShare
Liquid7100%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Homeoplex P71781-0007LiquidUnapproved homeopathic productsNovember 1, 2017
Homeoplex L71781-0006LiquidUnapproved homeopathic productsNovember 1, 2017
Homeoplex G71781-0005LiquidUnapproved homeopathic productsNovember 1, 2017
Homeoplex F71781-0004LiquidUnapproved homeopathic productsNovember 1, 2017
Homeoplex D71781-0003LiquidUnapproved homeopathic productsNovember 1, 2017
Homeoplex B71781-0002LiquidUnapproved homeopathic productsOctober 31, 2017
Homeoplex A71781-0001LiquidUnapproved homeopathic productsOctober 31, 2017

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.