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Data / Drug companies / Laboratoires M&L

Laboratoires M&L: 15 products in the FDA NDC directory, labeler code 10345

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

Laboratoires M&L (labeler code 10345) lists 15 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 15 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on September 1, 2025.

The request: Watch Laboratoires M&L (FDA labeler code 10345): 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
10345
Products in commercial distribution
15
Packages
36
Finished drugs by generic name
3
Prescription products
0
Over the counter products
15
Flagged as original packager
15 of 15 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
February 6, 2015
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 drugs15100%

Products by type

TypeProductsShare
Over the counter drugs15100%

Drugs it lists

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

DrugProductsCompanies listing it
Octinoxate, octisalate, titanium dioxide, zinc oxide102
Octinoxate, titanium dioxide, zinc oxide47
Octisalate, titanium dioxide, zinc oxide11

Dosage forms

Dosage formProductsShare
Cream1493.3%
Kit16.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
ERBORIAN CC Red Correct Color Correcting SPF 2510345-953CreamOver the counter monograph drugsSeptember 1, 2025
ERBORIAN CC CREME Color Correcting SPF 25 BRONZE10345-952CreamOver the counter monograph drugsSeptember 1, 2025
ERBORIAN CC CREME Color Correcting SPF 25 MEDIUM10345-951CreamOver the counter monograph drugsSeptember 1, 2025
ERBORIAN CC CREME Color Correcting SPF 25 FAIR10345-950CreamOver the counter monograph drugsSeptember 1, 2025
Erborian BB creme au Ginseng chocolate SPF 2010345-904CreamOver the counter monograph drugsMay 1, 2022
Erborian CC Dull Correct SPF2510345-914CreamOver the counter monograph drugsMay 27, 2019
Erborian cc creme high definition spf 25 caramel10345-913CreamOver the counter monograph drugsAugust 21, 2018
Erborian cc red correct spf 2510345-912CreamOver the counter monograph drugsJuly 1, 2018
ERBORIAN DOUBLE SAMPLE CC CREME CLAIR and DORE SPF 2510345-921KitOver the counter monograph drugsDecember 3, 2017
Erborian - bb creme au ginseng caramel spf2010345-903CreamOver the counter monograph drugsDecember 16, 2016
Erborian - bb creme nude spf2010345-902CreamOver the counter monograph drugsAugust 17, 2016
Erborian - cc creme high definition spf25 clair10345-911CreamOver the counter monograph drugsJuly 13, 2016
Erborian - cc creme high definition spf 2510345-910CreamOver the counter monograph drugsFebruary 6, 2015
Erborian - bb creme au ginseng dore spf 2010345-901CreamOver the counter monograph drugsFebruary 6, 2015
Erborian - bb creme au ginseng clair spf 2010345-900CreamOver the counter monograph drugsFebruary 6, 2015

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.