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Data / Drug companies / Sambria Pharmaceuticals, LLC

Sambria Pharmaceuticals, LLC: 20 products in the FDA NDC directory, labeler code 54723

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

Sambria Pharmaceuticals, LLC (labeler code 54723) lists 20 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 20 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 10, 2025.

The request: Watch Sambria Pharmaceuticals, LLC (FDA labeler code 54723): 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
54723
Products in commercial distribution
20
Packages
23
Finished drugs by generic name
5
Prescription products
0
Over the counter products
20
Flagged as original packager
20 of 20 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
August 15, 2013
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 drugs20100%

Products by type

TypeProductsShare
Over the counter drugs20100%

Drugs it lists

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

DrugProductsCompanies listing it
Lidocaine hydrochloride12134
Benzocaine4110
Lidocaine2216
Tetracaine14
Tetracaine hcl12

Dosage forms

Dosage formProductsShare
Cream1890%
Cloth15%
Liquid15%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
BeardedMoney54723-032CreamOver the counter monograph drugsJuly 10, 2025
Hello Sugar54723-031CreamOver the counter monograph drugsJuly 10, 2025
TattooNumb54723-030CreamOver the counter monograph drugsJune 24, 2025
Arte Maximum strength Numbing Cream54723-024CreamOver the counter monograph drugsFebruary 7, 2025
Tattoo Numbing Cream Co54723-023CreamOver the counter monograph drugsFebruary 7, 2025
Now Numb Numbing Cream54723-022CreamOver the counter monograph drugsNovember 29, 2024
Painless Tattoo Numbing Cream54723-020CreamOver the counter monograph drugsMay 9, 2024
Painless Tattoo Numbing54723-019LiquidOver the counter monograph drugsMay 9, 2024
Launch Medical54723-018CreamOver the counter monograph drugsFebruary 23, 2024
Painless Tattoo 354723-017CreamOver the counter monograph drugsSeptember 26, 2023
Painless Tattoo 254723-016CreamOver the counter monograph drugsSeptember 26, 2023
Painless Tattoo 154723-015CreamOver the counter monograph drugsSeptember 26, 2023
Pain free IV54723-008CreamOver the counter monograph drugsJuly 20, 2022
Ombre Men overtime wipes54723-007ClothOver the counter monograph drugsJanuary 1, 2022
NeuroMed FA54723-722CreamOver the counter monograph drugsAugust 21, 2017
NeuroMed Topical Anesthetic 754723-300CreamOver the counter monograph drugsAugust 1, 2016
NeuroMed FA54723-722CreamOver the counter monograph drugsFebruary 1, 2016
NeuroMed Topical Analgesic LA54723-310CreamOver the counter monograph drugsFebruary 1, 2016
NeuroMed Topical Anesthetic 754723-300CreamOver the counter monograph drugsAugust 20, 2015
NeuroMed 7 Topical Pain Relief54723-175CreamOver the counter monograph drugsAugust 15, 2013

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.